Instrumentation for manipulating artificial intervertebral disc trials having a cylindrical engagement surface

ABSTRACT

Instrumentation for implanting an artificial intervertebral disc includes a static trial holder for manipulating static trials, the static trial holder including an extension having a longitudinal axis, at least two prongs coupled to a fulcrum located at a distal extension end of the extension, each of the prongs having a prong extension, the prong extensions together defining a contractable and expandable holding enclosure for holding the static trial; and a sleeve that surrounds the distal extension and that is collinear with the extension longitudinal axis, and that is rotatable about the extension longitudinal axis; wherein rotation of the sleeve about the extension longitudinal axis brings an inner surface of the sleeve to bear on at least one of the prongs to move the holding enclosure to a contracted state in which the static trial cannot be removed from the holding enclosure.

CROSS-REFERENCE TO RELATED APPLICATIONS

The present application is a continuation application of U.S. patentapplication Ser. No. 10/282,356 (filed Oct. 29, 2002) entitled“Instrumentation and Methods For Use In Implanting an ArtificialIntervertebral Disc”, now U.S. Pat. No. 7,169,182 (“the '182 patent),which is a continuation-in-part application of U.S. patent applicationSer. No. 10/256,160 (filed Sep. 26, 2002) entitled “ArtificialIntervertebral Disc Having Limited Rotation Using a Captured Ball andSocket Joint With a Solid Ball and Compression Locking Post”, now U.S.Pat. No. 6,989,032 (“the '032 patent), which is a continuation-in-partapplication of U.S. patent application Ser. No. 10/175,417 (filed Jun.19, 2002) now U.S. Pat. No. 7,563,285 entitled “ArtificialIntervertebral Disc Utilizing a Ball Joint Coupling”, which is acontinuation-in-part application of U.S. patent application Ser. No.10/151,280 (filed May 20, 2002) entitled “Tension Bearing ArtificialDisc Providing a Centroid of Motion Centrally Located Within anIntervertebral Space”, which is a continuation-in-part application ofboth U.S. patent application Ser. No. 09/970,479 (filed Oct. 4, 2001)entitled “Intervertebral Spacer Device Utilizing a Spirally SlottedBelleville Washer Having Radially Extending Grooves”, now U.S. Pat. No.6,669,730 (“the '730 patent”) as well as U.S. patent application Ser.No. 10/140,153 (filed May 7, 2002) entitled “Artificial IntervertebralDisc Having a Flexible Wire Mesh Vertebral Body Contact Element”, nowabandoned the former being a continuation-in-part application of U.S.patent application Ser. No. 09/968,046 (filed Oct. 1, 2001) entitled“Intervertebral Spacer Device Utilizing a Belleville Washer HavingRadially Extending Grooves”, now abandoned and the latter being acontinuation-in-part application of both the '730 patent (detailedabove) as well as U.S. patent application Ser. No. 10/128,619 (filedApr. 23, 2002) entitled “Intervertebral Spacer Having a Flexible WireMesh Vertebral Body Contact Element”, now U.S. Pat. No. 6,863,689 (“the'689 patent”), which is a continuation-in-part application of both U.S.patent application Ser. No. 09/906,119 (filed Jul. 16, 2001) andentitled “Trial Intervertebral Distraction Spacers”, now U.S. Pat. No.6,607,559 (“the '559 patent”) as well as U.S. patent application Ser.No. 09/982,148 (filed Oct. 18, 2001) and entitled “Intervertebral SpacerDevice Having Arch Shaped Spring Elements”, now U.S. Pat. No. 6,673,113(“the '113 patent”). All of the above mentioned applications are herebyincorporated by reference herein in their respective entireties.

FIELD OF THE INVENTION

This invention relates generally to systems and methods for use in spinearthroplasty, and more specifically to instruments for distracting anintervertebral space, inserting and removing trial artificialintervertebral discs, and inserting, impacting, repositioning, levelingand extracting artificial intervertebral discs, and methods of usethereof.

BACKGROUND OF THE INVENTION

The bones and connective tissue of an adult human spinal column consistsof more than twenty discrete bones coupled sequentially to one anotherby a tri-joint complex that consists of an anterior disc and the twoposterior facet joints, the anterior discs of adjacent bones beingcushioned by cartilage spacers referred to as intervertebral discs.These more than twenty bones are anatomically categorized as beingmembers of one of four classifications: cervical, thoracic, lumbar, orsacral. The cervical portion of the spine, which comprises the top ofthe spine, up to the base of the skull, includes the first sevenvertebrae. The intermediate twelve bones are the thoracic vertebrae, andconnect to the lower spine comprising the five lumbar vertebrae. Thebase of the spine is the sacral bones (including the coccyx). Thecomponent bones of the cervical spine are generally smaller than thoseof the thoracic spine, which are in turn smaller than those of thelumbar region. The sacral region connects laterally to the pelvis. Whilethe sacral region is an integral part of the spine, for the purposes offusion surgeries and for this disclosure, the word spine shall referonly to the cervical, thoracic, and lumbar regions.

The spinal column is highly complex in that it includes these more thantwenty bones coupled to one another, housing and protecting criticalelements of the nervous system having innumerable peripheral nerves andcirculatory bodies in close proximity. In spite of these complications,the spine is a highly flexible structure, capable of a high degree ofcurvature and twist in nearly every direction.

Genetic or developmental irregularities, trauma, chronic stress, tumors,and degenerative wear are a few of the causes that can result in spinalpathologies for which surgical intervention may be necessary. Withrespect to the failure of the intervertebral disc, and the insertion ofimplants and/or height restorative devices, several methods and deviceshave been disclosed in the prior art that achieve immobilization and/orfusion of adjacent bones by implanting artificial assemblies in or onthe spinal column. More recently, the development of non-fusion implantdevices, which purport to permit continued natural movement in thetri-joint complex, have provided great promise as a preferablyalternative to fusion devices. The region of the back that needs to becorrected, as well as the individual variations in anatomy, determinethe appropriate surgical protocol and implantation assembly. Generally,the preparation of the intervertebral space for the receipt of fusion ornon-fusion devices involves removing the damaged disc material andthereafter distracting the adjacent vertebral bones to their appropriatedistance apart. Once the proper height of the intervertebral space isrestored, the fusion or non-fusion device can be implanted.

It is an object of the invention to provide instrumentation and methodsthat enable surgeons to more accurately, easily, and efficiently preparethe intervertebral space and implant fusion or non-fusion devices. Otherobjects of the invention not explicitly stated will be set forth andwill be more clearly understood in conjunction with the descriptions ofthe preferred embodiments disclosed hereafter.

SUMMARY OF THE INVENTION

The preceding objects are achieved by the invention, which includesstatic trial artificial intervertebral discs (sometimes referred toherein as a “static trial”), a static trial artificial intervertebraldisc holder (sometimes referred to herein as a “static trial holder”), adynamic trial artificial intervertebral disc (sometimes referred toherein as a “dynamic trial”), an artificial intervertebral discinserter/impactor (sometimes referred to herein as an“inserter/impactor”), an artificial intervertebral discrepositioner/extractor (sometimes referred to herein as a“repositioner/extractor”), and an artificial intervertebral disc leveler(sometimes referred to herein as a “leveler”).

More particularly, the systems and methods disclosed herein are intendedfor use in spine arthroplasty procedures, and specifically for use withthe systems and methods described herein in conjunction with the systemsand method described in U.S. patent application Ser. No. 10/256,160(filed Sep. 26, 2002) entitled “Artificial Intervertebral Disc HavingLimited Rotation Using a Captured Ball and Socket Joint With a SolidBall and Compression Locking Post” (hereinafter referred to as “the '160application”) as well as U.S. patent application Ser. No. 09/906,127(filed Jul. 16, 2001) entitled “Insertion Tool For Use WithIntervertebral Spacers” (hereinafter referred to as “the '127application”), both applications of which are mentioned above. However,it should be understood that the systems and methods described hereinare also suitable for use with other systems and methods withoutdeparting from the scope of the invention.

For example, while the static trials described herein are primarilyintended for use in determining the appropriate size of particularembodiments of the artificial intervertebral disc implants described inthe '160 application to be implanted (or whether a particular size canbe implanted) into the distracted intervertebral space, they can also beused for determining the appropriate size of any other suitablyconfigured orthopedic implant or trial to be implanted (or whether aparticular size can be implanted) into the distracted intervertebralspace.

And, for example, while the static trial holder described herein isprimarily intended for use in holding, inserting, removing, andotherwise manipulating the static trials described herein, it can alsobe used for manipulating any embodiment of the trial spacers describedin the '127 application (also referred to therein and herein asdistraction spacers), and can also be used for manipulating any othersuitably configured orthopedic device.

And, for example, while the dynamic trial described herein is primarilyintended for use in distracting an intervertebral space according to theprocedures described herein and/or for determining the appropriate sizeof particular embodiments artificial intervertebral disc implantsdescribed in the '160 application to be implanted (or whether aparticular size can be implanted) into the distracted intervertebralspace, it can also be used for distracting an intervertebral spaceaccording to other procedures and/or for determining the appropriatesize of any other suitably configured orthopedic implant or trial to beimplanted (or whether a particular size can be implanted) into thedistracted intervertebral space.

And, for example, while the inserter/impactor described herein isprimarily intended for use in holding, inserting, removing, impacting,extracting, and otherwise manipulating particular embodiments of theartificial intervertebral disc implants described in the '160application, it can also be used for manipulating any other suitablyconfigured orthopedic implant or trial.

And, for example, while the repositioners/extractors described herein isprimarily intended for use in repositioning and/or extracting and/orotherwise manipulating particular embodiments of the artificialintervertebral disc implants described in the '160 application, it canalso be used for manipulating any other suitably configured orthopedicimplant or trial.

And, for example, while the leveler described herein is primarilyintended for use in setting the proper position of, and/or otherwisemanipulating, particular embodiments of the artificial intervertebraldisc implants described in the '160 application, it can also be used formanipulating any other suitably configured orthopedic implant or trial.

While the instrumentation described herein (e.g., the static trials,static trial holder, dynamic trial, inserter/impactor,repositioners/extractors, and leveler) will be discussed for use withthe artificial intervertebral disc of FIGS. 1 g-n, such discussions aremerely by way of example and not intended to be limiting of their uses.Thus, it should be understood that the tools can be used with any of theartificial intervertebral discs disclosed in the '160 application, orany other artificial intervertebral disc having (or being modifiable ormodified to have) suitable features therefor. Moreover, it isanticipated that the features of the artificial intervertebral disc(e.g., the flat surfaces and accompanying holes) and/or the statictrials (e.g., the cylindrical trunks and flat surfaces and accompanyingholes) that are used by the tools discussed herein to hold and/ormanipulate these devices (such features, it should be noted, were firstshown and disclosed in the '160 application and the '127 application)can be applied, individually or collectively or in various combinations,to other trials, spacers, artificial intervertebral discs or otherorthopedic devices as stand-alone innovative features for enabling suchtrials, spacers, artificial intervertebral discs, or other orthopedicdevices to be more efficiently and more effectively held and/ormanipulated by the tools described herein or by other tools havingsuitable features. In addition, it should be understood that theinvention encompasses artificial intervertebral discs, spacers, trials(static or dynamic), and/or other orthopedic devices, that have one ormore of the features disclosed herein, in any combination, and that theinvention is therefore not limited to artificial intervertebral discs,spacers, trials, and/or other orthopedic devices having all of thefeatures simultaneously.

More particularly with regard to the static trials described herein, aplurality of static trials are provided primarily for use in determiningthe appropriate size of an artificial intervertebral disc to beimplanted (or whether a particular size of the artificial intervertebraldisc can be implanted) into the distracted intervertebral space (e.g.,the artificial intervertebral disc 160 of FIGS. 1 g-n). Preferably, foreach artificial intervertebral disc to be implanted, a plurality ofsizes of the artificial intervertebral disc would be available. That is,preferably, a plurality of the same type of artificial intervertebraldisc would be available, each of the plurality having a respective widthand depth dimension combination that allows it to fit within acorrespondingly dimensioned intervertebral space. For example, theplurality of artificial intervertebral discs could include artificialintervertebral discs having widths being either 35 mm or 40 mm, anddepths ranging from 14 mm to 18 mm in 1 mm increments, for a total of 10discs. Accordingly, preferably, each of the plurality of static trials100 for use with a particular plurality of differently sized artificialintervertebral discs would have a respective width and depth dimensionset corresponding to the width and depth of a respective one of theplurality of differently sized artificial intervertebral discs. Forexample, the plurality of static trials 100 for use with the set ofartificial intervertebral discs described for example could includestatic trials 100 having widths being either 35 mm or 40 mm, and depthsranging from 14 mm to 18 mm in 1 mm increments, for a total of 10 statictrials. It should be understood that the artificial intervertebral discsand/or the static trials 100 can be offered in a variety of dimensionswithout departing from the scope of the invention, and that thedimensions specifically identified and quantified herein are merelyexemplary. Moreover, it should be understood that the set of statictrials 100 need not include the same number of trials for eachartificial intervertebral disc in the set of artificial intervertebraldiscs, but rather, none, one, or more than one trial can be included inthe trial set for any particular artificial intervertebral disc in theset.

Each of the plurality of static trials preferably further includesfeatures that can be used by the static trial holder (described below),the inserter/impactor (described below), and therepositioners/extractors (described below). With regard to a featurethat can be used by the static trial holder, each static trialpreferably includes a recess that can be gripped by the opposingsemicircular extents of the static trial holder. Preferably, this recessforms an annular groove that establishes a cylindrical trunk between thebaseplates of the static trial, such that the baseplates extend asflanges from either end of the cylindrical trunk. Accordingly,preferably, the opposing semicircular extents each have a thicknesssmaller than the width of the annular groove, and as such fit into theannular groove to grip the cylindrical trunk between them.

With regard to features that can be used by the inserter/impactor, eachstatic trial (and each artificial intervertebral disc that the trialsapproximate) preferably includes an anteriorly facing flat surface,flanked by two anteriolaterally facing flat surfaces (one on each sideof the anteriorly facing flat surface), and, to provide for holding ofthe static trial or disc for an anterior insertion approach, a holespaced from the anteriorly facing flat surface, the hole having alongitudinal axis parallel to the anteriorly facing flat surface. Theholding pin of the inserter/impactor fits within the hole, and theangled flat surfaces of the static trial or disc fit against thecorrespondingly angled flat surfaces of the inserter/impactor, andoperation of the inserter/impactor pulls the holding pin toward the flatsurface of the inserter/impactor opposite the pin, to rigidly hold thestatic trial or disc by the baseplate. When the static trial is held inthis manner, rotation of the static trial or disc about a longitudinalaxis (e.g., in the case of the trials, an axis parallel to thelongitudinal axis of the cylindrical trunk) relative to theinserter/impactor is prevented by interference of the corners of thestatic trial's or disc's flat surfaces and the corners of theinserter/impactor's flat surfaces, similar to the manner in which awrench holding a nut prevents rotation of the nut relative to thewrench. Further, the holding of the static trial or disc in this mannerallows for some repositioning of the static trial or disc in theintervertebral space via rotation of the static trial or disc in eitherdirection about the longitudinal axis of the intervertebral space.

Preferably, both of the baseplates of the static trial or disc havesimilarly configured flat surfaces, and both baseplates' flat surfacesfit against the angled flat surfaces of the inserter/impactor to providefor a more secure holding of the static trial or disc by theinserter/impactor. Also preferably, in order to provide for a holding ofthe static trial or disc for two additional (here, anteriolateral)insertion approaches, each static trial or disc also include twoadditional holes, one spaced apart from one of the anteriolaterallyfacing flat surfaces, and the other spaced apart from the other of theanteriolaterally facing flat surfaces. Accordingly, operation of theinserter/impactor can fit the holding pin into either of these twoadditional holes, and hold the anteriolaterally facing flat surface (theone associated with the hole into which the pin is fit) of the statictrial or disc against the flat surface of the inserter/impactor oppositethe pin. It should be understood that preferably, in order to facilitatethese two additional approaches, the angle separating the anteriorlyfacing flat surface of the static trial or disc and one of theanteriolaterally facing flat surfaces of the static trial or disc isequal to the angle separating the anteriorly facing flat surface and theother of the anteriolaterally facing flat surfaces.

With regard to features that can be used by therepositioners/extractors, each static trial (and each artificialintervertebral disc that the trials approximate) preferably includes atleast two holes extending longitudinally into one of the baseplates ofthe trial or disc from the inwardly facing surface of the baseplate.More than two holes can be used to provide for multiplerepositioning/extracting approaches. Preferably, in order for the samerepositioning/extracting tool to be used for multiple approaches on thesame trial or artificial intervertebral disc, adjacent holes should beseparated by the same distance separating other adjacent holes.

As discussed in greater detail below with regard to therepositioners/extractors, in order to engage two of the holes, eachrepositioner/extractor has two pins extending in parallel from a centralshaft, perpendicular to the longitudinal axis of the central shaft. Thepins can be inserted into the holes, and pulling or pushing on thecentral shaft along its longitudinal axis when the holes are engagedpulls or pushes the static trial or artificial intervertebral disc inthe intervertebral space. Further, because two holes are engaged, thestatic trial or artificial intervertebral disc can be rotated in eitherdirection about a longitudinal axis passing through the intervertebralspace, by rotating of the central shaft of the repositioner/extractorabout its distal end, about an axis parallel to the longitudinal axes ofthe pins.

On each repositioner/extractor, the pins are formed on prongs thatextend laterally from the central shaft. The direction of the prongs,and the location of the pins relative to the central shaft, determinethe angle or angles of surgical approach for which a particularrepositioner/extractor can be used. Further, the number and location ofholes further determine the angle or angles of surgical approach forwhich a particular repositioner/extractor can be used. Accordingly, thepresent invention contemplates a variety of repositioner/ extractors,and a variety of holes configurations, to provide the surgeon with avariety of possible surgical approach angles.

As described in greater detail below, three repositioner/extractors areillustrated and described (symmetric, offset left, and offset right) forexample,, and, for example, two hole configurations are illustrated anddescribed. A first hole configuration includes the hole configurationdescribed above, that is, three holes on one of the baseplates (e.g.,the lower baseplate), the holes being configured so that a first hole islocated in the anterior-posterior plane, and the adjacent (second andthird) holes are located in respective opposing anteriolateral planes oneither side of the first hole. A second hole configuration includes fourholes on one of the baseplates (e.g., the upper baseplate), the holesbeing configured so that first and second holes straddle theanterior-posterior plane, a third hole is located so that the third holeand the first hole straddle one of the opposing anteriolateral planes,and a fourth hole is located so that the fourth hole and the second holestraddle the other of the opposing anteriolateral planes.

With further regard to the static trial holder described herein, thestatic trial holder is provided primarily for use in holding, inserting,removing, and otherwise manipulating the static trials described herein.Preferably, the static trial holder has a pair of opposing prongs thatopen away from one another and close toward one another. Each of theprongs has a semicircular extent and the semicircular extents face oneanother to define a circular holding enclosure that is useful forcapturing the cylindrical trunk of the static trial between them. Theprongs are spring biased toward a neutral position such that the holdingenclosure is spring biased to a receptive state in which the cylindricaltrunk can be snapped into (or out of) the holding enclosure bytemporarily placing the holding enclosure in an expanded state (byforcing the cylindrical trunk against the mouth of the enclosure) thatallows passage of the cylindrical trunk through the mouth of theenclosure. Once the cylindrical trunk is in the enclosure, the holdingenclosure can be placed in a contracted state, or locked, where thetrial is more securely held, so that the trial will not escape theholding enclosure as it is experiencing greater forces while beinginserted and removed from the intervertebral space. This locking iseffected by rotating a sleeve that surrounds the prongs. The bore of thesleeve is configured to press the prongs together when the sleeve isrotated a quarter turn, and to allow them to separate when the sleeve isagain rotated a quarter turn (in either direction). The sleeve is biasedtoward stopping its rotation at either the “locked” or “unlocked” statesof the holding enclosure, by the cooperation of recesses on theextension's outer surface and corresponding spring plungers radiallydisposed to project from the sleeve's inner surface. It should beunderstood that when the static trial is being held (either when theholding enclosure is in its receptive state or in its contracted state),because the semicylindrical extents fit within the annular groove of thestatic trial, the static trial will not escape from the enclosure alongthe longitudinal axis of the cylindrical trunk. While the static trialholder is discussed herein as primarily used for manipulating the statictrials, it preferably is also useful for manipulating the distractionspacers described in the '127 application, in that the semicircularextents of the pincers preferably also interact with the annular groovesand cylindrical trunks of those distraction spacers in the same manneras described herein.

With regard to the dynamic trial described herein, the dynamic trial isprovided primarily for distracting an intervertebral space according tothe procedures described herein and/or for determining the appropriatesize of an artificial intervertebral disc to be implanted (or whether aparticular size can be implanted) into the distracted intervertebralspace. While the distraction systems and methods described in the '127application are also useful for distracting an intervertebral space, thedynamic trial is provided as an additional or alternate distractiontool. Further, while the static trials described herein as useful fordetermining the appropriate size of an artificial intervertebral disc tobe implanted (or whether a particular size can be implanted), thedynamic trial is provided as an additional or alternate sizing tool.

The dynamic trial preferably includes a shaft having a bifurcated trialat a distal end. Each half of the bifurcated trial preferably has on itsoutwardly facing surface a convex dome that is shaped like the convexdome of the corresponding baseplate of the artificial intervertebraldisc that the dynamic trial approximates. The shaft includes an innershaft portion that centrally divides into upper and lower distalextensions that, from the point of division to their distal ends, areeach biased toward positions in which they converge toward one another.The lower distal extension is connected to the lower half of thebifurcated trial, and the upper distal extension is connected to theupper half of the bifurcated trial. Preferably, the upper half isadjustably connected to the upper distal extension by a pivot pin thatallows the upper half to rotate about a lateral axis that passes throughthe longitudinal and lateral center of the bifurcated trial. This axisof rotation allows the upper half, when separating from the lower half,to adjust to the orientation of the upper vertebral bone without causingthe bone to hinge relative to the lower vertebral bone. In order toeffect the separation of the upper and lower halves, the shaft furtherincludes an outer shaft potion that is translatable adjacent the innershaft portion, the outer shaft portion having a pin that passes betweenthe distal extensions.

The outer shaft portion is preferably translatable distally by theforward movement of a control knob near the proximal end of the shaft,and translatable proximally by backward movement of the control knob. Asthe outer shaft portion is pushed distally, the pin is pushed distallyto overcome the bias of the divided extensions to separate them andcorrespondingly separate the halves of the bifurcated trial. Preferably,markings are provided on the inner shaft portion to quantify the depth(to which the bifurcated trial has been expanded) corresponding to thedistance that the outer shaft portion has been translated with respectto the inner shaft portion. It is anticipated that the pushing forcerequired to separate the halves will increase as they separate, due tothe compression of the spine seeking to close the intervertebral spaceand the annulus seeking to prevent the adjacent vertebral discs fromseparating beyond a certain point. Therefore, to provide a mechanicaladvantage to the operator in the event that greater distraction isrequired, but the operator cannot push the control knob farther withunaided human effort, an fine control knob is provided. The fine controlknob is preferably threaded onto the proximal end of the inner shaftportion, proximal to the control knob. Thus, rotation of the finecontrol knob about the longitudinal axis of the inner shaft portion willcause the body of the fine control knob to press against the controlknob to move it farther distally. The interference of the threads of thefine control knob-inner shaft portion interface prevents the finecontrol knob from backing up proximally unless the fine control knob isreverse rotated to effect that result. Finally, the proximal end of theshaft is preferably flanged to serve as a slap hammer for impaction, ifnecessary for proper positioning of the bifurcated trial, and/or forcedextraction of the bifurcated trial.

With further regard to the inserter/impactor described herein, theinserter/impactor is provided primarily for holding, inserting,repositioning, removing, impacting, extracting, and otherwisemanipulating an artificial intervertebral disc (or static trial) havingfeatures suitable for being manipulated by the inserter/impactor.Exemplary suitable artificial intervertebral discs are described in the'160 application with regard to FIGS. 8 a-y, 9 a-t, 10 a-t, 11 a-j, and12 a-o thereof and by the accompanying descriptions therefor (e.g.,embodiments identified as the first, second, third, fourth, and fifthpreferred embodiments of the fourth embodiment family, etc.). Regardingthe features suitable for being manipulated by the inserter/impactor,such features include those discussed above as being suitable featureson the static trials and artificial intervertebral disc, namely, ananteriorly facing flat surface on the second (e.g., lower) baseplate ofthe trial or disc, flanked by two anteriolaterally facing flat surfaces(one on each side of the anteriorly facing flat surface), and, toprovide for holding of the trial or disc for an anterior insertionapproach, a hole spaced from the anteriorly facing flat surface, thehole having a longitudinal axis parallel to the anteriorly facing flatsurface.

The inserter/impactor includes a shaft having a distal end that hasangled flat surfaces corresponding to and fittable against the angledflat surfaces of the static trial or artificial intervertebral disc, anda holding pin that extends from the center flat surface along alongitudinal axis of the shaft, the pin having a distal end that bendsdownward. The holding pin is spring loaded in a central channel of theshaft, so that it is biased toward and against the central flat surface(preferably, the bent end of the pin prevents it from entering thecentral channel). A flange, mechanically connected to the pin andtranslating adjacent the shaft, can be pushed distally to overcome thebias of the spring to space the pin away from the central flat surface.In this position, the pin can be inserted in the hole in the baseplateof the artificial intervertebral disc. Releasing the knob allows thespring to pull the pin back, causing the anteriorly facing surface ofthe baseplate to be held against the central flat surface of theinserter/impactor and the anteriolaterally facing flat surfaces of theartificial intervertebral disc to be held against the othercorresponding flat surfaces of the inserter/impactor. A knob on theinserter/impactor can be rotated about the longitudinal axis of theshaft to pull the pin tighter and lock its position to more securelyhold the baseplate, and reverse rotated to unlock and loosen the pin.

When the static trial or artificial intervertebral disc is held in thismanner, rotation of the trial or disc about its longitudinal axisrelative to the inserter/impactor is prevented by interference of thecorners of the trial's or disc's flat surfaces and the corners of theinserter/impactor's flat surfaces, similar to the manner in which awrench holding a nut prevents rotation of the nut relative to thewrench. Further, the holding of the trial or disc in this manner allowsfor some repositioning of the trial or disc in the intervertebral spacevia rotation of the trial or disc in either direction about thelongitudinal axis of the intervertebral space.

Preferably, both of the baseplates of the static trial or disc havesimilarly configured and oriented flat surfaces, and both baseplates'flat surfaces fit against the angled flat surfaces of theinserter/impactor, to provide for a more secure holding of the statictrial or disc by the inserter/impactor.

Also preferably, in order to provide for a holding of the static trialor disc for two additional (here, anteriolateral) insertion approaches,each static trial or disc also includes two additional holes, one spacedapart from one of the anteriolaterally facing flat surfaces, and theother spaced apart from the other of the anteriolaterally facing flatsurfaces. Accordingly, operation of the inserter/impactor can fit theholding pin into either of these two additional holes, and hold theassociated anteriolaterally facing flat surface (the one associated withthe hole into which the pin is fit) of the static trial or disc againstthe flat surface of the inserter/impactor opposite the pin. It should beunderstood that preferably, in order to facilitate these two additionalapproaches, the angle separating the anteriorly facing flat surface ofthe static trial or disc and one of the anteriolaterally facing flatsurfaces of the static trial or disc is equal to the angle separatingthe anteriorly facing flat surface and the other of the anteriolaterallyfacing flat surfaces.

Also preferably, as shown the baseplates of each of the plurality ofstatic trials are appropriately lordotically angled relative to oneanother to ease insertion of the static trial or artificialintervertebral disc into the intervertebral space and to mimic how theartificial intervertebral disc will typically be oriented as it is beinginserted.

With further regard to the repositioners/extractors described herein,each repositioner/extractor is provided primarily for repositioningand/or extracting a static trial or artificial intervertebral dischaving features suitable for being manipulated by therepositioner/extractor. Exemplary suitable artificial intervertebraldiscs are described in the '160 application with regard to FIGS. 8 a-y,9 a-t, 10 a-t, 11 a-j, and 12 a-o thereof and by the accompanyingdescriptions therefor (e.g., embodiments identified as the first,second, third, fourth, and fifth preferred embodiments of the fourthembodiment family, etc.). Regarding the features suitable for beingmanipulated by each repositioner/extractor, such features include atleast two holes extending longitudinally into one of the baseplates ofthe static trial or artificial intervertebral disc from the inwardlyfacing surface of the baseplate. More than two holes can be used toprovide for multiple repositioning/extracting approaches. Preferably, inorder for the same repositioning/extracting tool to be used for multipleapproaches on the same trial or artificial intervertebral disc, adjacentholes should be separated by the same distance separating other adjacentholes.

In order to engage the two holes, each repositioner/extractor has twopins extending in parallel from a central shaft, perpendicular to thelongitudinal axis of the central shaft. The pins are spaced to engagethe two holes simultaneously, and each pin has a diameter smaller thanthe diameter of the hole it is to engage. Therefore, the pins can beinserted into the holes, and pulling or pushing on the central shaftalong its longitudinal axis when the holes are engaged pulls or pushesthe static trial or artificial intervertebral disc in the intervertebralspace. Further, because two holes are engaged, the static trial orartificial intervertebral disc can be rotated in either direction abouta longitudinal axis passing through the intervertebral space, byrotating of the central shaft of the repositioner/extractor about itsdistal end, about an axis parallel to the longitudinal axes of the pins.A handle at a proximal end of the central shaft is useful for pushing orpulling on the shaft. A flange adjacent the proximal end of the shaft isuseful for impaction (either with a distally directed force or aproximally directed force), if necessary to manipulate the shaft.

On each repositioner/extractor, the pins are formed on prongs thatextend laterally from the central shaft. The direction of the prongs,and the location of the pins relative to the central shaft, determinethe angle or angles of surgical approach for which a particularrepositioner/extractor can be used. Further, the number and location ofholes further determine the angle or angles of surgical approach forwhich a particular repositioner/extractor can be used. Accordingly, thepresent invention contemplates a variety of repositioner/extractors, anda variety of holes configurations, to provide the surgeon with a varietyof possible surgical approach angles.

With further regard to the leveler described herein, the leveler isprovided primarily for establishing a parallel orientation of thebaseplates (relative to one another), and/or securing the purchase ofthe stabilizing spikes, of an artificial intervertebral disc havingfeatures suitable for being manipulated by the leveler. Exemplarysuitable artificial intervertebral discs are described in the '160application with regard to FIGS. 8 a-y, 9 a-t, 10 a-t, 11 a-j, and 12a-o thereof and by the accompanying descriptions therefor (e.g.,embodiments identified as the first, second, third, fourth, and fifthpreferred embodiments of the fourth embodiment family, etc.). Regardingthe features suitable for being manipulated by the leveler, suchfeatures include suitably formed inwardly facing surfaces of thebaseplates of the artificial intervertebral disc.

More particularly, the leveler includes a shaft having a forked distalend formed by two opposing tongs that are symmetric to one another abouta longitudinal axis of the shaft. Each of the tongs has an extent thatinitially curves laterally outward away from the shaft and from theother tong's extent, to define a central pocket forward of the shaftbetween the tongs' extents. Each tong's extent then resumes a distaldirection to become parallel to the shaft and to the other tong'sextent.

Each tong's extent has an upper surface and a lower surface. The uppersurface is preferably shaped to conform against the inwardly facingsurface of a first (e.g., upper) baseplate of an artificialintervertebral disc, and the lower surface is preferably shaped toconform against the inwardly facing surface of a second (e.g., lower)baseplate of the artificial intervertebral disc, so that insertion ofthe forked distal end of the leveler between the baseplates, with thecentral pocket of the distal end avoiding the central portion of theartificial intervertebral disc, and with the upper and lower surfaces soengaging the inwardly facing surfaces of the baseplates, causes thebaseplates to be placed in parallel orientation with respect to oneanother. A handle is provided at a proximal end of the shaft forpushing, pulling, and otherwise manipulating the leveler as needed.

When the artificial intervertebral disc is inserted into theintervertebral space, its baseplates will typically be lordoticallyangled with respect to one another. The leveler can be applied to theartificial intervertebral disc to bring the baseplates parallel to oneanother. The forked distal end of the leveler is inserted so that thetongs' extents are placed between the inwardly facing surfaces of thebaseplates, and so that the central pocket of the leveler avoids thatportion of the artificial intervertebral disc that joins the baseplates.As the leveler is inserted, the tongs act as wedges to force theposterior portions of the baseplates away from one another. Accordingly,as the posterior portions are being separated, the stabilizing spikes onthe outwardly facing surfaces of the baseplates find or secure theirpurchase in the hard bone of the outer ring of the vertebral bodyendplates. When the forked distal end is fully seated, the extents ofthe tongs hold the baseplates parallel to one another, and so that thespikes are fully engaged in the endplates.

BRIEF DESCRIPTION OF THE DRAWINGS

FIGS. 1 a-f show front (FIG. 1 a), side (FIG. 1 b), perspective (FIG. 1c), top (FIG. 1 d), bottom cutaway (FIG. 1 e), and top cutaway (FIG. 1f) views of a static trial of the present invention.

FIGS. 1 g-n show front (FIG. 1 g), side cutaway (FIG. 1 h), top (FIG. 1i), side cutaway (FIG. 1 j), bottom cutaway (FIG. 1 k), top cutaway(FIG. 1 l), bottom perspective (FIG. 1 m), and top perspective (FIG. 1n), views of an exemplary artificial intervertebral disc of the presentinvention.

FIGS. 2 a-l show top (FIG. 2 a), side (FIG. 2 b), perspective (FIG. 2c), disassembly (FIG. 2 d-j), and side cutaway (FIG. 2 k-l) views of astatic trial holder of the present invention.

FIGS. 3 a-d show side (FIG. 3 a), top (FIG. 3 b), side cutaway (FIG. 3c), and perspective (FIG. 3 d) views of a dynamic trial of the presentinvention.

FIGS. 4 a-d show side (FIG. 4 a), top. (FIG. 4 b), side cutaway (FIG. 4c), and perspective (FIG. 4 d) views of an inserter/impactor of thepresent invention.

FIGS. 4 e-h show side (FIG. 4 e), top (FIG. 4 f, side cutaway (FIG. 4g), and perspective (FIG. 4 h) views of an inserter/impactor of thepresent invention holding a static trial of the present invention.

FIGS. 4 i-j show top views of an inserter/impactor of the presentinvention holding a static trial of the present invention in twoalternative ways.

FIGS. 4 k-n show side (FIG. 4 k), top (FIG. 4 l), side cutaway (FIG. 4m), and perspective (FIG. 4 n) views of an inserter/impactor of thepresent invention holding an exemplary artificial intervertebral disc ofthe present invention.

FIGS. 4 o-p show top views of an inserter/impactor of the presentinvention holding an exemplary artificial intervertebral disc of thepresent invention in two alternative ways.

FIGS. 5 a-c show side (FIG. 5 a), top (FIG. 5 b), and perspective (FIG.5 c) views of a symmetric repositioner/extractor of the presentinvention.

FIGS. 5 d-f show side (FIG. 5 d), top (FIG. 5 e), and perspective (FIG.5 f) views of an offset left repositioner/extractor of the presentinvention.

FIGS. 5 g-i show side (FIG. 5 g), top (FIG. 5 h), and perspective (FIG.5 i) views of an offset right repositioner/extractor of the presentinvention.

FIGS. 5 j-l show side (FIG. 5 j), top (FIG. 5 k), and perspective (FIG.5 l) views of an alternative offset left repositioner/extractor of thepresent invention.

FIGS. 5 m-o show side (FIG. 5 m), top (FIG. 5 n), and perspective (FIG.5 o) views of an alternative offset right repositioner/extractor of thepresent invention.

FIGS. 5 p-u show exemplary various possible repositioner/extractorapproach angles with a three hole configuration of the presentinvention.

FIGS. 5 v-dd show exemplary various possible repositioner/extractorapproach angles with a four hole configuration of the present invention.

FIGS. 6 a-d bottom (FIG. 6 a), side (FIG. 6 b), front (FIG. 6 c), toppartial perspective (FIG. 6 d), and bottom partial perspective (FIG. 6e) views of a leveler of the present invention.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

While the invention will be described more fully hereinafter withreference to the accompanying drawings, it is to be understood at theoutset that persons skilled in the art may modify the invention hereindescribed while achieving the functions and results of the invention.Accordingly, the descriptions that follow are to be understood asillustrative and exemplary of specific structures, aspects and featureswithin the broad scope of the invention and not as limiting of suchbroad scope. Like numbers refer to similar features of like elementsthroughout.

A preferred embodiment of a static trial of the present invention, and apreferred embodiment of an artificial intervertebral disc of the presentinvention, both for use with the instrumentation of the presentinvention, will now be described.

Referring now to FIGS. 1 a-f, a static trial of the present invention isshown in front (FIG. 1 a), side (FIG. 1 b), perspective (FIG. 1 c), top(FIG. 1 d), bottom cutaway (FIG. 1 e) and top cutaway (FIG. 1 f) views.Referring now to FIGS. 1 g-n, an artificial intervertebral disc of thepresent invention is shown in front (FIG. 1 g), side cutaway (FIG. 1 h),top (FIG. 1 i), side cutaway (FIG. 1 j), bottom cutaway (FIG. 1 k), topcutaway (FIG. 1 l), bottom perspective (FIG. 1 m), and top perspective(FIG. 1 n) views.

It should be understood that the illustration and reference herein tothe artificial intervertebral disc shown in FIGS. 1 g-n is merely toshow an example of one type of artificial intervertebral disc that iscontemplated by, encompassed by, and suitable for use with, the presentinvention, and that such illustration and reference herein is not meantto limit the scope of the present invention or limit the uses of thepresent invention. Rather, any other artificial intervertebral disc (orany other orthopedic device) having suitable features for beingmanipulated by the instrumentation and methods described herein arecontemplated by the present invention. Indeed, the features suitable formanipulation (e.g., angled flat surfaces with adjacent holes) areencompassed by the present invention, regardless of to what orthopedicdevice they may be applied. Other exemplary suitable artificialintervertebral discs include, but are not limited to, the artificialintervertebral discs described in the '160 application with regard toFIGS. 8 a-y, 9 a-t, 10 a-t, 11 a-j, and 12 a-o thereof and by theaccompanying descriptions therefor (e.g., embodiments identified as thefirst, second, third, fourth, and fifth preferred embodiments of thefourth embodiment family, etc.). It should be noted that, as can be seenfrom FIGS. 1 g-n, that the artificial intervertebral disc shown in FIGS.1 g-n has features similar to those of these other suitable artificialintervertebral discs of the '160 application, and it should beunderstood that such similar features are structurally and functionallyas described in the '160 application. Such similar features include aninwardly facing surface 164 a of the upper baseplate 164 a, and a convexstructure 162 on the lower baseplate 168 b, the convex structure 162having an inwardly facing surface 164 b.

And, while the instrumentation described herein (e.g., the statictrials, static trial holder, dynamic trial, inserter/impactor,repositioners/extractors, and leveler) will be discussed for use withthe artificial intervertebral disc of FIGS. 1 g-n, such discussions aremerely by way of example and not intended to be limiting of their uses.Thus, it should be understood that the tools can be used with any of theartificial intervertebral discs disclosed in the '160 application, orany other artificial intervertebral disc having (or being modifiable ormodified to have) suitable features therefor. Moreover, it isanticipated that the features of the artificial intervertebral disc(e.g., the flat surfaces and accompanying holes) and/or the statictrials (e.g., the cylindrical trunks and flat surfaces and accompanyingholes) that are used by the tools discussed herein to hold and/ormanipulate these devices (such features, it should be noted, were firstshown and disclosed in the '160 application and the '127 application)can be applied, individually or collectively or in various combinations,to other trials, spacers, artificial intervertebral discs or otherorthopedic devices as stand-alone innovative features for enabling suchtrials, spacers, artificial intervertebral discs, or other orthopedicdevices to be more efficiently and more effectively held and/ormanipulated by the tools described herein or by other tools havingsuitable features. In addition, it should be understood that theinvention encompasses artificial intervertebral discs, spacers, trials(static or dynamic), and/or other orthopedic devices, that have one ormore of the features disclosed herein, in any combination, and that theinvention is therefore not limited to artificial intervertebral discs,spacers, trials, and/or other orthopedic devices having all of thefeatures simultaneously.

A plurality of static trials 100 are provided primarily for use indetermining the appropriate size of an artificial intervertebral disc tobe implanted (or whether a particular size of the artificialintervertebral disc can be implanted) into the distracted intervertebralspace (e.g., the artificial intervertebral disc 160 of FIGS. 1 g-n).Preferably, for each artificial intervertebral disc to be implanted, aplurality of sizes of the artificial intervertebral disc would beavailable. That is, preferably, a plurality of the same type ofartificial intervertebral disc would be available, each of the pluralityhaving a respective width and depth dimension combination that allows itto fit within a correspondingly dimensioned intervertebral space. Forexample, the plurality of artificial intervertebral discs could includeartificial intervertebral discs having widths being either 35 mm or 40mm, and depths ranging from 14 mm to 18 mm in 1 mm increments, for atotal of 10 discs. Accordingly, preferably, each of the plurality ofstatic trials 100 for use with a particular plurality of differentlysized artificial intervertebral discs would have a respective width anddepth dimension set corresponding to the width and depth of a respectiveone of the plurality of differently sized artificial intervertebraldiscs. For example, the plurality of static trials 100 for use with theset of artificial intervertebral discs described for example couldinclude static trials 100 having widths being either 35 mm or 40 mm, anddepths ranging from 14 mm to 18 mm in 1 mm increments, for a total of 10static trials. It should be understood that the artificialintervertebral discs and/or the static trials 100 can be offered in avariety of dimensions without departing from the scope of the invention,and that the dimensions specifically identified and quantified hereinare merely exemplary. Moreover, it should be understood that the set ofstatic trials 100 need not include the same number of trials for eachartificial intervertebral disc in the set of artificial intervertebraldiscs, but rather, none, one, or more than one trial can be included inthe trial set for any particular artificial intervertebral disc in theset.

Each of the static trials (the static trial 100 shown is exemplary forall of the static trials in the plurality of static trials; preferablythe static trials in the plurality differ from one another only withregard to overall dimensions as described above) includes at least onefeature that can be gripped by a tool. Suitable tools include, but arenot limited to, the static trial holder 200 described below, theinserter/impactor 400 described below, and the repositioners/extractors510,520,530,540 described below. Specifically, the static trial 100includes a recess 102 that can be gripped by the opposing semicircularextents 216 a-b of the static trial holder 200. Preferably, this recess102 forms an annular groove 104 that establishes a cylindrical trunk 106between the upper and lower baseplates 108 a-b of the static trial 100,such that the baseplates 108 a-b extend as flanges 110 a-b from eitherend of the cylindrical trunk 106. Accordingly, preferably, the opposingsemicircular extents 216 a-b each have a thickness smaller than thewidth of the annular groove 104, and as such fit into the annular groove104 to grip the cylindrical trunk 106 between them.

In some embodiments, while not shown in FIGS. 1 a-f, it is alsopreferable that the annular groove 104 radially widen outwardly, suchthat the walls 112 of the annular groove 104 are tapered toward oneanother with the increasing depth of the groove 104, such that the floor114 of the groove 104 is more narrow than the opening 116 of the groove104. Accordingly, preferably, in such embodiments, each semicircularextent 216 a-b correspondingly radially widens outwardly, such that thethinner portion of the extent 216 a-b fits closer to the floor 114 ofthe annular groove 104, so that the tapered surfaces of the extents 216a-b compress against the tapered walls 112 of the annular groove 104when the static trial 100 is gripped by the static trial holder 200.This taper locking provides for a secure grip so that the static trial100 can be manipulated accurately and efficiently.

In some embodiments, while not shown in FIGS. 1 a-f, it is alsopreferable that the floor of the annular groove 104 of the cylindricaltrunk 106 be ridged (e.g., have ridges that run parallel to thelongitudinal axis of the cylindrical trunk), and the surfaces of thesemicircular extents 216 a-b of the static trial holder 200 thatcompress against the floor of the annular groove 104 when the statictrial holder 200 grips the static trial 100 be correspondingly providedwith ridges. The interlocking of the ridges of the static trial 100 withthe ridges of the static trial holder 200 when the static trial 100 isgripped prevents rotation of the static trial 100 about the longitudinalaxis of the cylindrical trunk 106 with respect to the static trialholder 200.

Additionally with regard to features that can be gripped by a tool, eachof the static trials includes at least one feature that can be grippedby a tool that preferably is also used to grip the artificialintervertebral disc that the trial approximates. Suitable tools that cangrip both the trial and the artificial intervertebral disc include, butare not limited to, the inserter/impactor 400 described below.Specifically, for being gripped by the inserter/impactor 400, eachstatic trial 100 and artificial intervertebral disc 160 includes ananteriorly facing flat surface 120 b,180 b, flanked by twoanteriolaterally facing flat surfaces 120 a,180 a and 120 c,180 c (oneon each side of the anteriorly facing flat surface 120 b,180 b), and, toprovide for holding of the static trial 100 or disc 160 for an anteriorinsertion approach, a hole 122 b,182 b spaced from the anteriorly facingflat surface, the hole 122 b,182 b having a longitudinal axis parallelto the anteriorly facing flat surface 120 b,180 b.

The holding pin 408 of the inserter/impactor 400 fits within the hole122 b,182 b, and the angled flat surfaces 120 a-c,180 a-c of the statictrial 100 or disc 160 fit against the correspondingly angled flatsurfaces 420 a-c of the inserter/impactor 400, and operation of theinserter/impactor 400 pulls the holding pin 408 toward the flat surface120 b,180 b of the inserter/impactor 400 opposite the pin 408, torigidly hold the static trial 100 or disc 160 by the structure of thestatic trial 100 or disc 160 having the hole 122 b,182 b (e.g., thebaseplate 108 b,168 b). When the static trial 100 or disc 160 is held inthis manner, rotation of the static trial 100 or disc 160 about alongitudinal axis (of the static trial 100 or disc 160) relative to theinserter/impactor 400 is prevented by interference of the corners of thestatic trial's 100 or disc's 160 flat surfaces 120 a-c,180 a-c and thecorners of the inserter/impactor's 400 flat surfaces 420 a-c, similar tothe manner in which a wrench holding a nut prevents rotation of the nutrelative to the wrench. Further, the holding of the static trial 100 ordisc 160 in this manner allows for some repositioning of the statictrial 100 or disc 160 in the intervertebral space via rotation of thestatic trial 100 or disc 160 in either direction about the longitudinalaxis of the intervertebral space.

Preferably, both of the baseplates of the static trial 100 or disc 160have similarly configured flat surfaces. For example, the lowerbaseplate's 108 b,168 b flat surfaces 120 a-c,180 a-c have similarlyconfigured and similarly oriented counterpart flat surfaces 120 d-f, 180d-f on the upper baseplate 108 a,168 a. Further preferably, bothbaseplates' 108 a-b,168 a-b flat surfaces 120 a-f,180 a-f face theangled flat surfaces 420 a-c of the inserter/impactor 400 when thestatic trial 100 or disc 160 is held by the inserter/impactor 400. Forexample, as discussed below with regard to the inserter/impactor 400, inan anterior approach for the trial 100 (as shown in FIGS. 4 e-h), 120 aand 120 d facing 420 a, 120 b and 120 e facing 420 b, and 120 c and 120f facing 420 c, and in an anterior approach for the disc 160 (as shownin FIGS. 4 k-n), 180 a and 180 d facing 420 a, 180 b and 180 e facing420 b, and 180 c and 180 f facing 420 c.

It should be noted that preferably, when the static trial 100 is held bythe inserter/impactor 400, the flat surfaces 120 a-c and the counterpartflat surfaces 120 d-f are tightly held against the angled flat surfaces420 a-c of the inserter/impactor 400 as described above. It is alsopreferable that the baseplates 108 a-b of each of the plurality ofstatic trials 100 be appropriately lordotically angled relative to oneanother to ease insertion of the static trial 100 into theintervertebral space and to mimic how the artificial intervertebral disc160 will typically be oriented as it is being inserted using theinserter/impactor 400, and to ease insertion of the static trial 100into the intervertebral space. While not shown in FIGS. 1 a-f, in someembodiments, when the static trials 100 are formed in such alordotically oriented configuration, it is preferable that the flatsurfaces 120 d-f on the first (e.g., upper) baseplate 108 a be parallelto the flat surfaces 120 a-c of the second (e.g., lower) baseplate 108 bin the static trial's 100 appropriately lordotically orientedconfiguration, so that when the static trial 100 is held tightly by theinserter/impactor 400, the flat surfaces 120 a-f are flush with the flatsurfaces 420 a-c of the inserter/impactor 400 even though the baseplates108 a-b are lordotically angled with respect to one another.

By contrast, preferably, when the artificial intervertebral disc 160 isheld by the inserter/impactor 400, the flat surfaces 180 a-c are tightlyheld against the angled flat surfaces 420 a-c of the inserter/impactor400 as described above, but the counterpart flat surfaces 180 d-f areloosely held against the angled flat surfaces 420 a-c of theinserter/impactor 400. As such, the structure of the artificialintervertebral disc 160 having the counterpart flat surfaces 180 d-f(e.g., the upper baseplate 168 a) is able to angulate and rotate to alimited extent relative to the structure of the artificialintervertebral disc 160 having the flat surfaces 180 a-c. This permitsthe artificial intervertebral disc 160 to adjust to the intervertebralspace (e.g., to the angulation of the adjacent vertebral endplates,defining the intervertebral space, relative to one another) as it isbeing inserted thereinto. That is, typically, the adjacent vertebralendplates will be lordotically angled with respect to one another as aresult of the intervertebral space being prepared and distracted. As theartificial intervertebral disc 160 is then inserted into theintervertebral space using the inserter/impactor 400, then, thebaseplates 168 a-b will be permitted to lordotically angle with respectto one another to squeeze into the intervertebral space.

Also preferably, in order to provide for a holding of the static trial100 or disc 160 for two additional (here, anteriolateral) insertionapproaches, each static trial 100 or disc 160 also includes twoadditional holes 122 a,182 a and 122 c,182 c, one (e.g., 122 a,182 a)spaced apart from one of the anteriolaterally facing flat surfaces(e.g., 120 a,180 a), and the other (e.g., 122 c,182 c) spaced apart fromthe other of the anteriolaterally facing flat surfaces (e.g., 120 c,180c). Accordingly, operation of the inserter/impactor 400 can fit theholding pin 408 into either of these two additional holes 122 a,182 a or122 c,182 c, and hold the associated anteriolaterally facing flatsurface (the one associated with the hole into which the pin 408 is fit)of the static trial 100 or disc 160 against the flat surface of theinserter/impactor 400 opposite the pin 408. For example, as discussedbelow with regard to the inserter/impactor 400, in a firstanteriolateral approach for the trial 100 (as shown in FIG. 4 i), 120 aand 120 d facing 420 b, 120 b and 120 e not confronted, and 120 c and120 f facing 420 a, and a first anteriolateral approach for the disc 160(as shown in FIG. 4 o), 180 a and 180 d facing 420 b, 180 b and 180 enot confronted, 180 c and 180 f facing 420 a. And, for example, asdiscussed below with regard to the inserter/impactor 400, in a secondanteriolateral approach for the trial 100 (as shown in FIG. 4 j), 120 aand 120 d facing 420 c, 120 b and 120 e facing 420 a, and 120 c and 120f not confronted, and a second anteriolateral approach for the disc 160(as shown in FIG. 4 p), 180 a and 180 d facing 420 c, 180 b and 180 efacing 420 a, 180 c and 180 f not confronted.

It should be understood that preferably, in order to facilitate theseadditional approaches, the angle separating the anteriorly facing flatsurface of the static trial 100 or disc 160 and one of theanteriolaterally facing flat surfaces of the static trial 100 or disc160 is equal to the angle separating the anteriorly facing flat surfaceand the other of the anteriolaterally facing flat surfaces. Preferably,the surfaces are angled with respect to one another at an angle of 33.4degrees.

It should also be understood that the inclusion of additional adjacentangulated surfaces (or placing the angulated surfaces in other locationson the trial or disc), and/or including corresponding holes adjacent tosuch surfaces, can provide the surgeon with additional approaches, e.g.,other anteriolateral approaches, directly lateral approaches,posteriolateral approaches, and/or directly posterior approaches. Forexample, a trial or disc can have angled surfaces (and correspondingholes) along the entire perimeter of one or both of the baseplates, andthus enable the surgeon to engage the trial or disc from a number ofangles, including anterior, posterior, lateral, anteriolateral, andposteriolateral angles.

Additionally with regard to features that can be gripped by a tool, eachof the static trials includes at least one feature that can be grippedby a tool that preferably is also used to grip the artificialintervertebral disc that the trial approximates. Suitable tools that cangrip both the trial and the artificial intervertebral disc include, butare not limited to, the repositioners/extractors 500,510,520,530,540described below. Specifically, for being gripped by therepositioners/extractors, each static trial 100 and artificialintervertebral disc 160 includes at least two holes extendinglongitudinally into one of the baseplates of the static trial 100 orartificial intervertebral disc 160 from the inwardly facing surface ofthe baseplate. More than two holes can be used to provide for multiplerepositioning/extracting approaches. Preferably, in order for the samerepositioning/extracting tool to be used for multiple approaches on thesame trial or artificial intervertebral disc, adjacent holes should beseparated by the same distance separating other adjacent holes.

As discussed in greater detail below with regard to therepositioners/extractors 500,510,520,530,540, in order to engage two ofthe holes, each repositioner/extractor has two pins extending inparallel from a central shaft, perpendicular to the longitudinal axis ofthe central shaft. The pins are spaced to engage the two holessimultaneously, and each pin has a diameter smaller than the diameter ofthe hole it is to engage. Therefore, the pins can be inserted into theholes, and pulling or pushing on the central shaft along itslongitudinal axis when the holes are engaged pulls or pushes the statictrial or artificial intervertebral disc in the intervertebral space.Further, because two holes are engaged, the static trial or artificialintervertebral disc can be rotated in either direction about alongitudinal axis passing through the intervertebral space, by rotatingof the central shaft of the repositioner/extractor about its distal end,about an axis parallel to the longitudinal axes of the pins. A handle ata proximal end of the central shaft is useful for pushing or pulling onthe shaft. A flange adjacent the proximal end of the shaft is useful forimpaction (either with a distally directed force or a proximallydirected force), if necessary to manipulate the shaft.

On each repositioner/extractor, the pins are formed on prongs thatextend laterally from the central shaft. The direction of the prongs,and the location of the pins relative to the central shaft, determinethe angle or angles of surgical approach for which a particularrepositioner/extractor can be used. Further, the number and location ofholes further determine the angle or angles of surgical approach forwhich a particular repositioner/extractor can be used. Accordingly, thepresent invention contemplates a variety of repositioner/extractors, anda variety of holes configurations, to provide the surgeon with a varietyof possible surgical approach angles.

As described in greater detail below, three repositioner/extractors areillustrated and described (symmetric, offset left, and offset right) forexample,, and, for example, two hole configurations are illustrated anddescribed. Referring again to FIGS. 1 a-n, a first hole configurationincludes the hole configuration described above, that is, three holes onone of the baseplates (e.g., the lower baseplate 108 b,168 b), the holesbeing configured so that a first hole 122 b,182 b is located in theanterior-posterior plane, and the adjacent (second 122 a,182 a and third122 c,182 c) holes are located in respective opposing anteriolateralplanes on either side of the first hole 122 b,182 b. (This holeconfiguration is also shown in FIGS. 5 p-u, each of which shows a topcutaway view of the artificial intervertebral disc 160 of FIGS. 1 g-n,showing its lower baseplate 168 b, having the first hole configuration,engaged by one of the repositioners/extractors 500,510,520. Each view ofthe lower baseplate 168 b shows the first hole 182 b, the second hole182 a, and the third hole 182 c of the first hole configuration.)

Referring again to FIGS. 1 a-n, a second hole configuration includesfour holes on one of the baseplates (e.g., the upper baseplate 108 a,168a), the holes being configured so that first (e.g., 130 c,190 c) andsecond (e.g., 130 b,190 b) holes straddle the anterior-posterior plane,a third hole (e.g., 130 d,190 d) is located so that the third hole andthe first hole straddle one of the opposing anteriolateral planes, and afourth hole (e.g., 130 a,190 a) is located so that the fourth hole andthe second hole straddle the other of the opposing anteriolateralplanes. (This hole configuration is also shown in FIGS. 5 v-dd, each ofwhich shows a bottom cutaway view of the artificial intervertebral discof FIGS. 1 g-n, showing its upper baseplate 168 a, having the secondhole configuration, engaged by one of the repositioners/extractors500,510,520. Each view of the upper baseplate shows the first hole 190c, the second hole 190 b, the third hole 190 d, and the fourth hole 190a, of the second hole configuration.)

It should be understood that configurations having more or fewer holes,and in a variety of locations, are contemplated by the invention, andthe detailed descriptions of only two hole configurations is not meantto limit the invention to only these two configurations. Importantly,the invention encompasses using a hole or any number of holes, bored atany suitable angle, whether parallel to other holes or not, in anynumber of locations on a spacer, a trial or an artificial intervertebraldisc (not limited to locations on the baseplates), for purposes ofenabling the spacer, trial, or disc to be gripped by a manipulationinstrument (not limited to a repositioner/extractor) that engages thehole, and/or to enable the surgeon to work from a variety of approaches.For example, as described in more detail below, the first and secondhole configurations described herein, in cooperation with therepositioner/extractors, provide the surgeon with the ability to workfrom a directly anterior approach, as well as several anteriolateralapproaches. It should be understood that additional hole configurationscan enable the surgeon to work from a directly posterior approach,posteriolateral approaches, directly lateral approaches, oranteriolateral approaches that are different that those illustrated. Forexample, the placement of one or more suitably spaced holes (or theaddition of one or more holes) on the posterior edge, and/or one or bothof the lateral edges of one or both of the baseplates, would enable thesurgeon to use the repositioner/extractors of the present invention toachieve such approaches.

Thus, it can be seen that each of the repositioner/extractors can beused in more than one manner depending on the tool desired and theapproach desired. These manners are described in greater detail belowand illustrated in FIGS. 5 p-dd with regard to the detailed descriptionof the repositioners/extractors.

Also preferably, the baseplates 108 a-b of each of the plurality ofstatic trials 100 preferably has a convex dome 124 a-b on its outwardlyfacing surface 126 a-b that is shaped like the convex dome 184 a-b onthe outwardly facing surface 186 a-b of the corresponding baseplate 168a-b of the artificial intervertebral disc 160 that the static trial 100approximates. Preferably, each convex dome 124 a-b is smooth, ratherthan having a porous coating that is preferred for the convex domes 184a-b of the artificial intervertebral disc 160, and each outwardly facingsurface 126 a-b does not have stabilizing spikes such as the stabilizingspikes 188 a-b on the outwardly facing surfaces 186 a-b of theartificial intervertebral disc 160. The omission of these devicestabilizing and bone ingrowth encouraging structures and surfaces on thestatic trials 100 enables the surgeon to test the size of the artificialintervertebral disc 160 to be implanted without traumatically engagingthe vertebral body endplates.

Accordingly, the surgeon can prepare and distract the intervertebralspace, and then insert and remove at least one of the static trials (ormore, as necessary) to find the size that is most appropriate for theintervertebral space.

A preferred embodiment of a static trial holder of the present inventionwill now be described.

Referring to FIGS. 2 a-c and 2 k, a static trial holder of the presentinvention is shown in side (FIG. 2 a), top (FIG. 2 b), perspective (FIG.2 c), and side cutaway (FIG. 2 k) views. In addition, referring to FIGS.2 d-f, a sleeve of the static trial holder is shown in side cutaway(FIG. 2 d), front (FIG. 2 e), and back (with partial cutaway) (FIG. 2 f)views. In addition, referring to FIGS. 2 g-i, an extension of the statictrial holder is shown in top (FIG. 2 g), proximal cutaway (FIG. 2 h),side (FIG. 2 i), and distal cutaway (FIG. 2 j) views.

The static trial holder 200 is provided primarily for use in holding,inserting and removing the static trials described herein, ordistraction spacers having suitable features therefor, such as thedistraction spacers disclosed in the '127 application.

More specifically, the static trial holder 200 includes a handle 202, anextension 204, and a sleeve 206. As shown in FIG. 2 k, the handle 202and the extension 204 are fixed to one another (preferably by the distalend of the handle 202 being fixed to the proximal end of the extension204) to form a shaft 208. The sleeve 206 surrounds the extension 204 andis rotatable with respect to the handle 202 and the extension 204 aboutthe longitudinal axis of the shaft 208. The handle 202 preferably has anflange 232 at its proximal end for use in applying a distally orproximally directed force to get the static trial 100 (or distractionspacer) into or out of the intervertebral space, and/or for use inhelping the surgeon rotate the sleeve 206 with respect to the extension204 (by gripping the flange 232 and the control knob 219 describedbelow).

The distal end of the extension 204 forms a contractable and expandableholding enclosure 210 in that the distal end is divided at a fulcrum 212into two prongs 214 a-b, each of which terminates in a semicircularextent 216 a-b, each of which has a tapered end 215 a-b. The extents 216a-b are oriented such that the tapered ends 215 a-b face one another todefine a radially inwardly tapering mouth 213, and such that thesemicircular openings oppose one another to define the holding enclosure210. The prongs 214 a-b are spring biased toward a neutral position(preferably by the formation of the fulcrum 212 in combination with thestrength of the material of which the extension 204 is made) such thatthe holding enclosure 210 is spring biased to a receptive state(described below), but the prongs 214 a-b can be brought together tocontract the holding enclosure 210 to a contracted state, (describedbelow) or the prongs 214 a-b can be further separated to expand theholding enclosure 210 to an expanded state (described below).

When the holding enclosure 210 is in the receptive state, the width ofthe mouth 213 of the holding enclosure 210 does not accommodate thediameter of the cylindrical trunk 106 of the static trial 100 (ordistraction spacer) for passage therethrough. However, from thisreceptive state, the mouth 213 can be temporarily widened (placing theholding enclosure 210 in its expanded state) to accommodate the diameter(for passage of the cylindrical trunk 106 through the mouth 213), if asufficient force is applied to overcome the neutral position bias of theprongs 214 a-b and thus widen the mouth 213. (Preferably, there isenough space between the outer surfaces of the prongs 214 a-b and theinner surface of the bore 218 of the sleeve, when the prongs 214 a-b arein their neutral position, so that the prongs 214 a-b can be separatedwithout interference.) The sufficient force can be applied by pressingthe cylindrical trunk 106 against the tapered ends 215 a-b of the mouth213, in that the separating force component of the radially inward forceof the pressing will be applied to the semicircular extents 216 a-b bythe taper of the tapered ends 215 a-b. Because the holding enclosure 210is biased toward the receptive state, after the cylindrical trunk 106 ispassed through the mouth 213 and into the holding enclosure 210, theholding enclosure 210 will return to its receptive state in which thewidth of the mouth 213 does not allow passage of the cylindrical trunk106 without the sufficient force. Preferably, the force required towiden the mouth 213 is greater than gravity and/or the greatest forcethat will be experienced by moving the static trial holder 200 prior toplacing the holding enclosure 210 in the contracted state. Therefore,once the cylindrical trunk 106 is in the holding enclosure 210, evenbefore the holding enclosure 210 is placed in its contracted state, thecylindrical trunk 106 will not escape the holding enclosure 210 as thestatic trial holder 200 is oriented with the holding enclosure 210downward, or is moved about.

It should be understood that when the static trial 100 (or distractionspacer) is being held (either when the holding enclosure 210 is in itsreceptive state or in its contracted state discussed below), because thesemicylindrical extents 216 a-b fit within the annular groove 104 of thestatic trial 100 (or distraction spacer), the static trial 100 (ordistraction spacer) will not escape from the enclosure along thelongitudinal axis of the cylindrical trunk 106. That is, as noted above,the recess 102 of each static trial 100 (or distraction spacer) forms anannular groove 104 that establishes the cylindrical trunk 106 betweenthe baseplates of the static trial (or distraction spacer), such thatthe baseplates extend as flanges from either end of the cylindricaltrunk 106. Accordingly, preferably, the opposing semicircular extentseach have a thickness smaller than the width of the annular groove 104,and as such fit into the annular groove 104 to grip the cylindricaltrunk 106 between them.

In some embodiments, while not shown in FIGS. 1 a-f or FIGS. 2 a-k, itis preferable that the annular groove 104 radially widen outwardly, suchthat the walls of the annular groove 104 taper toward one another withthe increasing depth of the groove, such that the floor of the groove ismore narrow than the opening 116 of the groove. Accordingly, preferably,in such embodiments, each semicircular extent 216 a-b correspondinglyradially widens outwardly, such that the thinner portion of the extent216 a-b fits closer to the floor of the annular groove 104, so that thetapered surfaces 215 a-b of the extents 216 a-b compress against thetapered walls of the annular groove 104 when the static trial 100 isgripped by the static trial holder 200. This taper locking provides fora secure grip so that the static trial 100 can be manipulated accuratelyand efficiently.

In some embodiments, while not shown in FIGS. 1 a-f or FIGS. 2 a-k, itis also preferable that the floor of the annular groove 104 of thecylindrical trunk 106 be ridged (e.g., have ridges that run parallel tothe longitudinal axis of the cylindrical trunk), and the surfaces of thesemicircular extents 216 a-b of the static trial holder 200 thatcompress against the floor of the annular groove 104 when the statictrial holder 200 grips the static trial 100 be correspondingly providedwith ridges. The interlocking of the ridges of the static trial 100 withthe ridges of the static trial holder 200 when the static trial 100 isgripped prevents rotation of the static trial 100 about the longitudinalaxis of the cylindrical trunk 106 with respect to the static trialholder 200.

In order to more tightly hold the static trial 100 (or distractionspacer) for manipulation of the static trial 100 (or distraction spacer)during surgical procedures in which greater forces will be experiencedby the static trial 100 (or distraction spacer) and the static trialholder 200, the holding enclosure 210 can be placed in a contractedstate. The holding enclosure 210 can be considered “unlocked” in itsreceptive or expanded states, and “locked” in its contracted state, withrespect to the nature of the hold that the static trial holder 200potentially can have or has on the cylindrical trunk 106. Preferably,when the holding enclosure 210 is locked, a force greater than thatwhich is applicable by an unaided surgeon or nurse (i.e., that which canbe applied to remove the cylindrical trunk 106 from the holdingenclosure 210 when the holding enclosure 210 is in its receptive state),and greater than that which will be experienced by the static trial 100(or distraction spacer) and the static trial holder 200 during surgicalprocedures) would be required to pull the cylindrical trunk 106 out ofthe holding enclosure 210. The placement of the holding enclosure 210 inits locked state or unlocked state is effected by operation of a holdingassembly that includes the extension 204 and the sleeve 206 and themanner in which they are configured and interact.

More particularly, the prongs 214 a-b can be brought together, to lockthe holding enclosure 210, by a rotation of the sleeve 206 with respectto the handle 202 and the extension 204 about the longitudinal axis ofthe shaft 208. A rotation control knob 219 is provided to ease therotation of the sleeve 206. As shown in FIGS. 2 g and 2 i-j in view ofFIGS. 2 d-e, the bore 218 of the sleeve 206 (shown in cutaway in FIG. 2e) defines a cross-section that has a width 220 that is greater than itsdepth 222. Further as shown in those figures, the prongs 214 a-b whenseparated (shown in cutaway in FIG. 2 j) define a cross-section having awidth 224 that is greater than its depth 226, the width 224 and depth226 of the prongs' cross-section being closely accommodated by the width220 and depth 222 of the bore's cross-section. When the prongs 214 a-bare together, the width of prongs' cross-section is closely accommodatedby the depth 222 of the bore's cross-section. Thus, when the sleeve 206is rotated with respect to the extension 204, the sides of the boredefining the depth 222 of its cross-section bear against the sides ofthe prongs 214 a-b, defining the width of their cross-section.

It should be noted that in order to ease the rotation of the sleeve 210so that the side of the bore 218, can bear against the sides of theprongs 214 a-b, the corners of the bore 218 are radiused, and at leastthe sides (that face away from one another) of the prongs 214 a-b arecurved. Preferably, as shown, the prongs 214 a-b when separated define apartial cylindrical cross-section. The effect of the bearing (of thesides of the bore 218 against the sides of the prongs 214 a-b) is borneby the space between the prongs 214 a-b, so that the space narrows andthe prongs 214 a-b are brought toward one another until they areaccommodated within the bore's depth 222. The bringing together of theprongs 214 a-b brings the semicircular extents 216 a-b together to placethe holding enclosure 210 into its contracted state, locking it.

Preferably, the sleeve 206 is biased toward establishing the holdingenclosure 210 in either an unlocked position or a locked position.Stated alternatively, when the holding enclosure 210 is unlocked (orlocked), the force required to begin rotation of the sleeve 206 isgreater than the force required to continue rotating the sleeve 206 oncerotation has begun. And, as the sleeve 206 is rotated toward a positionthat will unlock (or lock), the holding enclosure 210, it is biasedtoward stopping its rotation at that upcoming position. Statedalternatively, as the sleeve 206 is being rotated, the force required torotate the sleeve 206 past that upcoming position is greater than theforce that is required to rotate it prior to reaching that upcomingposition.

This biasing of the sleeve 206 toward positions that will either unlockor lock the holding enclosure 210 is effected by the inclusion of atleast one spaced recess 228 on the outer surface of the extension 204,and at least one radial bore 230 through the wall of the sleeve 206(preferably through the rotation control knob 219 as shown), which bores230 each have secured therein a spring plunger 232 (it should beunderstood that functionally equivalent devices can also be used inplace of a spring plunger). Preferably, each recess 228 is associatedwith a respective cooperating bore 230 and spring plunger 232. When agiven bore 230 (and spring plunger) is aligned with its associatedrecess 228, the sleeve 206 is in a position at which the holdingenclosure 210 is either unlocked or locked. Each of the spring plungers232 is biased radially inwardly from the inner surface of the sleeve206, and as such presses against the outer surface of the extension 204as the sleeve 206 is being rotated. Thus, when a recess 228 is presentedto the spring plunger 232, it plunges into the recess 228, stopping therotation of the sleeve 206. In order to restart (or continue) rotationof the sleeve 206, the bias of the spring plunger 232 must be overcomewhen the restarting (or continuing) rotational force is applied. Inorder to lower the overcoming force required to restart or continue therotation, the end of the spring plunger 232 is preferably convexlycurvate, and the recess is concavely curvate. Preferably, four recesses228 and bores 230 (and spring plungers) are provided, each pairrepresenting one of four quarter-turn rotated positions of the sleeve206. At each position of the sleeve 206, all four plungers 232 plungeinto the recesses 228, securing the sleeve 206 at that position until asufficient force is applied to overcome their plunging bias.

Accordingly, the static trials 100 of the invention (or distractionspacers such as those disclosed in the '127 application) can be held andmanipulated with the static trial holder 200. Holding the handle 202 ofthe static trial holder 200 in one hand, an operator can push thecylindrical trunk 106 of the static trial 100 (or the distractionspacer) against the mouth 213 of the holding enclosure 210 with enoughforce to temporarily expand the mouth 213 to a width that willaccommodate the diameter of the cylindrical trunk 106 for passagethrough the mouth 213. The radially inward tapering of the sides of themouth 213 (the facing ends 215 a-b of the semicircular extents 216 a-bof the prongs 214 a-b) facilitates this insertion. Once the cylindricaltrunk 106 has passed into the holding enclosure 210, the operator canlet go of the static trial 100 (or distraction spacer) because theprongs 214 a-b will be overcome by their bias toward their neutral stateand thus hold the static trial 100 in the holding enclosure 210 toprevent the static trial 100 from falling out or slipping out as thestatic trial holder 200 is moved with the static trial 100 prior toclosing (e.g., locking) the holding enclosure 210. (When the statictrial 100 (or distraction spacer) is being held in this manner, and theholding enclosure 210 is unlocked, the static trial 100 can be removedfrom the holding enclosure 210 by a pulling of the static trial 100through the mouth 213 of the holding enclosure 210 with a force requiredto again temporarily overcome the bias of the prongs 214 a-b towardtheir neutral state, to separate them and make the width of the mouth213 accommodate the diameter of the cylindrical trunk 106.)

Once the operator is ready to lock the holding enclosure 210, whilestill gripping the handle 202 of the static trial holder 200, he rotatesthe rotation control knob 219 either clockwise or counterclockwise tomove the sleeve 206 to the next quarter-turn position. If the rotationcontrol knob 219 is rotated with enough force to cause the springplungers 232 in the bores 230 to back out of the recesses 228, thesleeve 206 will rotate as desired. Once the sleeve 206 has reached thenext quarter-turn position, the spring plungers 232 will find therecesses 228 associated with that position, and plunge into the recesses228 to snap the sleeve 206 into the proper position. As the sleeve 206rotates, the sides of the sleeve's bores s inner surface bear againstthe curved outer surfaces of the prongs 214 a-b to push the prongs 214a-b together so that they are accommodated by the depth 222 of the bore218. When the prongs 214 a-b are pressed against one another and held inthat closed position by the maintenance of the sleeve 206 in the newposition (maintained by the spring plungers 232 in the recesses 228),the semicircular extents 216 a-b move toward one another and arecorrespondingly maintained together about the cylindrical trunk 106.When the prongs 214 a-b are held in this manner, the cylindrical trunk106 cannot be removed through the mouth 213 of the now-tighter (e.g.,locked) holding enclosure 210 without the application of forcespreferably greater than will be encountered when inserting and removingthe static trial 100 from the intervertebral space during the surgicalprocedures. Once the static trial 100 has been inserted and removed fromthe intervertebral space (or the distraction spacer has been insertedand removed from the intervertebral space after being used to distractthe space), the operator can lock the holding enclosure 210 by rotatingthe sleeve 206 another quarter turn (in either the clockwise or thecounterclockwise direction). Again, if the rotation control knob 219 isrotated with enough force to cause the spring plungers 232 to back outof the recesses 228, the sleeve 206 will rotate as desired. Once thesleeve 206 has reached the next quarter-turn position, the springplungers 232 will find the recesses 228 associated with that position,and plunge into the recesses 228 to snap the sleeve 206 into the properposition. As the sleeve 206 rotates, the sides of the sleeve's bores'sinner surface move away from the curved outer surfaces of the prongs 214a-b and allow the prongs 214 a-b to separate (under their own biastoward the neutral position) as they are accommodated by the width 220of the bore 218. When the prongs 214 a-b are separated and allowed toremain in that position by the maintenance of the sleeve 206 in the newposition (maintained by the spring plungers 232 in the recesses 228),the semicircular extents 216 a-b are separated from one another and holdthe cylindrical trunk 106 against falling or slipping out. That is, thecylindrical trunk 106 can be removed by the operator if the operatorapplies a sufficient force to widen the mouth 213 of the holdingenclosure 210 enough to let the cylindrical trunk 106 pass through themouth 213. Once the static trial 100 (or distraction spacer) is removed,another one can be inserted and manipulated if required.

Accordingly, the static trial holder 200 can be used to insert andremove the distraction spacers of the '127 application to distract theintervertebral space as described in the '127, and thereafter (or duringthe distraction) hold to insert and remove the static trials 100 to findthe appropriate size of artificial intervertebral disc to be implanted.

A preferred embodiment of a dynamic trial of the present invention willnow be described.

Referring now to FIGS. 3 a-d, a dynamic trial of the present inventionis shown in top (FIG. 3 a), side (FIG. 3 b), side cutaway (FIG. 3 c) andperspective (FIG. 3 d) views.

The dynamic trial 300 is provided primarily for distracting anintervertebral space according to the procedures described herein and/orfor determining the appropriate size of an artificial intervertebraldisc to be implanted (or whether a particular size can be implanted)into the distracted intervertebral space. While the distraction systemsand methods described in the '127 application are also useful fordistracting an intervertebral space, the dynamic trial 300 is providedas an additional or alternate distraction tool. Further, while thestatic trials described herein as useful for determining the appropriatesize of an artificial intervertebral disc to be implanted (or whether aparticular size can be implanted), the dynamic trial 300 is provided asan additional or alternate sizing tool.

More specifically, the dynamic trial 300 includes a shaft 302 having abifurcated trial 304 at a distal end of the shaft 302. The trial 304 hasan exterior that is preferably formed like the artificial intervertebraldisc that it is meant to approximate. Accordingly, each half 306 a-b ofthe bifurcated trial 304 has on its outwardly facing surface a convexdome 308 a-b that is shaped like the convex dome of the correspondingbaseplate of the artificial intervertebral disc that the dynamic trial300 approximates (e.g., the convex domes 184 a-b of the baseplates 168a-b of the artificial intervertebral disc 160 of FIGS. 1 g-n).Preferably, each convex dome 308 a-b is smooth, rather than having aporous coating that is preferred for the convex domes 184 a-b of theartificial intervertebral disc 160, and each half 306 a-b does not havestabilizing spikes such as the stabilizing spikes 188 a-b on theoutwardly facing surfaces 186 a-b of the artificial intervertebral disc160. The omission of these device stabilizing and bone ingrowthencouraging structures and surfaces on the dynamic trial 300 enables thesurgeon to test the size of the artificial intervertebral disc 160 to beimplanted without invading the vertebral body endplates. The shaft 302includes an inner shaft portion 310 that centrally divides at a fulcrum311 into upper and lower distal extensions 312 a-b. The lower distalextension 312 b is fixed to the upper distal extension 312 a at thefulcrum 311, preferably by screws 313 a-b that are plug welded in place.Preferably, as shown, at least the most proximal screw 313 b extendsabove the top surface of the upper distal extension 312 a to serve as abackup stop to prevent extreme forward movement of the control knob 318that is operated to separate the distal extensions 312 a-b (describedbelow).

From the point of division to their distal ends, each of the upper andlower distal extensions 312 a-b are spring biased (preferably by theformation of the fulcrum 311 in combination with the strength of thematerial of which the extensions 312 a-b are made, although the use ofother types of springs is contemplated by the present invention) towardpositions in which they converge toward one another (in the figures, theextensions 312 a-b are shown in these positions). The lower distalextension 312 b is connected (preferably fixed as shown) to the lowerhalf 306 b of the bifurcated trial 304, and the upper distal extension312 a is connected to the upper half 306 a of the bifurcated trial 304.Preferably, as shown, the upper half 306 a is adjustably connected tothe upper distal extension 312 a by a pivot pin 315 that allows theupper half 306 a to rotate about a lateral axis that passes through thelongitudinal and lateral center of the bifurcated trial 304. This axisof rotation allows the upper half 306 a, when separating from the lowerhalf 306 b, to adjust to the orientation of the upper (adjacent)vertebral bone without causing the bone to hinge relative to the lowervertebral bone (the bone adjacent the lower half 306 b).

In order to effect the separation of the upper and lower halves 306 a-b,the shaft 302 further includes an outer shaft potion 314 that islongitudinally translatable adjacent the inner shaft portion 310. Theouter shaft portion 314 preferably straddles the inner shaft portion 310as shown, and includes a pin 316 that passes between the distalextensions 312 a-b. The outer shaft portion 314 is preferablytranslatable distally by the forward movement of a control knob 318 nearthe proximal end of the shaft 302, and translatable proximally bybackward movement of the control knob 318. That is, when the controlknob 318 is pushed distally, the outer shaft portion 314 is movesdistally, and accordingly the pin 316 moves distally. If the pushingforce is great enough to overcome the bias of the divided extensions 312a-b (their bias toward one another), the divided extensions 312 a-b willseparate as the pin 316 moves between them (to make room for the pin316). The separation of the extensions 312 a-b will correspondinglyseparate the halves 306 a-b of the bifurcated trial 304. It should beunderstood that preferably, if the control knob 318 is released, thebias of the divided extensions 312 a-b will press against the pin 316,causing the pin 316 (and correspondingly the outer shaft portion 314 andthe control knob 318) to move proximally to allow the divided extensions312 a-b to return to their biased position, which will bring the halves306 a-b of the trial 304 back together so they can be removed from theintervertebral space. Preferably, markings 320 are provided on the innershaft portion 310 (preferably on its top surface so that the surgeon canmore easily see the markings 320) to quantify the depth (to which thebifurcated trial 304 is expanded) corresponding to the distance that theouter shaft portion 314 is translated with respect to the inner shaftportion 310.

It is anticipated that the pushing force required to separate the halves306 a-b will increase as they separate, due to the compression of thespine seeking to close the intervertebral space and the annulus seekingto prevent the adjacent vertebral discs from separating beyond a certainpoint. Therefore, to provide a mechanical advantage to the operator inthe event that greater distraction is required, but the operator cannotpush the control knob 318 farther with unaided human effort, an finecontrol knob 322 is provided. The fine control knob 322 is preferablythreaded onto the proximal end of the inner shaft portion 310, proximalto the control knob 318. Thus, rotation of the fine control knob 322about the longitudinal axis of the inner shaft portion 310 will causethe body of the fine control knob 322 to press against the control knob318 to move it farther distally. The interference of the threads of thefine control knob-inner shaft portion interface prevents the finecontrol knob 322 from backing up proximally unless the fine control knob322 is reverse rotated to effect that result.

Preferably, as shown, the proximal end 324 of the shaft 302 ispreferably flanged to serve as a slap hammer for impaction (by hittingthe proximal end 324 with a mallet with a distally directed force,e.g.), if necessary for proper positioning of the bifurcated trial 304,and/or forced extraction of the bifurcated trial 304 (by hitting theflange of the proximal end 324 with a mallet with a proximally directedforce, e.g.).

Accordingly, the dynamic trial 300 can be used as an additional oralternative distracting tool (e.g., to the distraction spacers), and/oras an alternative or additional sizing tool (e.g., to the statictrials). As an example of a use for the dynamic trial 300 as analternative or additional distraction tool and an alterative sizingtool, once the intervertebral space is distracted to (or, withoutdistraction, is at) a depth that is at least equal to the depth of theclosed bifurcated trial 304, the bifurcated trial 304 of the dynamictrial 300 can be inserted into the intervertebral space. (If theintervertebral space must be distracted initially because it starts outmore shallow than the depth of the closed bifurcated trial 304, thedistraction spacers of the '127 application and the methods disclosedtherein can be used, e.g.) The control knob 318 and/or fine control knob322 can be operated to separate the halves 306 a-b of the bifurcatedtrial 304 to distract the space as clinically appropriate. Because thebifurcated trial 304 is shaped externally to approximate the artificialintervertebral disc to be implanted (e.g., the artificial intervertebraldisc 160), and because the pivoting of the upper half 306 a of thebifurcated trial 304 allows the halves 306 a-b to appropriatelylordotically orient themselves, when the surgeon determines theintervertebral space to be distracted to its proper dimension (based onhow much compression is being experienced on the dynamic trial 300 andhow tight the annulus is), he can read the markings 320 on the shaft 302to determine what size of artificial intervertebral disc 160 is suitablefor the dimensioned intervertebral space. A subsequent bringing togetherof the halves 306 a-b and a removal of the dynamic trial 300 can then befollowed by insertion of the appropriately sized artificialintervertebral disc 160 (e.g., in a manner described below with regardto the inserter/impactor 400).

As an example of a use for the dynamic trial 300 as an alternativedistraction tool and an additional sizing tool, after the surgeon hasinitially distracted the intervertebral space (preferably with thedistraction spacers of the '127 application), and applied one or more ofthe static trials 100 to the intervertebral space to determine theappropriate size of the artificial intervertebral disc to be implanted(e.g., the artificial intervertebral disc 160), the surgeon can applythe dynamic trial 300, expand it to the size of the static trial 100that was determined to be the appropriate size for the intervertebralspace, and then further open the dynamic trial 300 for a final sizing.An example of a final sizing that would be useful would be to test theamount of farther distraction that is clinically possible, withouthaving to remove and replace static trials 100 when the compressionforce of the spine and the tension force of the annulus are at theirhigher levels. Also, the surgeon may wish to distract the space slightlymore than the size of the appropriately sized static trial 100 orartificial intervertebral disc 160, so that the artificialintervertebral disc 160 can be more easily inserted after removal of thestatic 100 or dynamic trial 300 results in a compressive settling of theintervertebral space. The surgeon may also wish to distract the spaceslightly more than the size of the appropriately sized static trial 100or artificial intervertebral disc 160, to prepare it for easy insertionof the artificial intervertebral disc 160 to be implanted, withconsideration for the height of the stabilizing spikes 188 a-b on theoutwardly facing surfaces 186 a-b of the baseplates 168 a-b of theartificial intervertebral disc 160. While the artificial intervertebraldisc 160 having the spikes 188 a-b can be implanted without theadditional distraction, some surgeons may find such additionaldistraction useful or desirable for a particular case.

A preferred embodiment of an inserter/impactor of the present inventionwill now be described.

Referring now to FIGS. 4 a-d, an inserter/impactor of the presentinvention is shown in side (FIG. 4 a), top (FIG. 4 b), side cutaway(FIG. 4 c) and perspective (FIG. 4 d) views. FIGS. 4 e-h show side (FIG.4 e), top (FIG. 4 f), side cutaway (FIG. 4g), and perspective (FIG. 4 h)views of an inserter/impactor of the present invention holding a statictrial of the present invention. FIGS. 4 i-j show top views of aninserter/impactor of the present invention holding a static trial of thepresent invention in two alternative ways. FIGS. 4 k-n show side (FIG. 4k), top (FIG. 4 l), side cutaway (FIG. 4 m), and perspective (FIG. 4 n)views of an inserter/impactor of the present invention holding anexemplary artificial intervertebral disc of the present invention. FIGS.4 o-p show top views of an inserter/impactor of the present inventionholding an exemplary artificial intervertebral disc of the presentinvention in two alternative ways.

The inserter/impactor 400 is provided primarily for holding, inserting,repositioning, removing, impacting, extracting, and otherwisemanipulating an artificial intervertebral disc having features suitablefor being manipulated by the inserter/impactor. (However, it can also beused to hold, insert, reposition, remove, impact, extract, and otherwisemanipulate the static trials 100 as described above, as well as anyother orthopedic device having suitable features therefor.) Exemplarysuitable artificial intervertebral discs include, but are not limitedto, the artificial intervertebral disc 160 described herein and theartificial intervertebral discs described in the '160 application withregard to FIGS. 8 a-y, 9 a-t, 10 a-t, 11 a-j, and 12 a-o thereof and bythe accompanying descriptions therefor (e.g., embodiments identified asthe first, second, third, fourth, and fifth preferred embodiments of thefourth embodiment family, etc.). Regarding the features suitable forbeing manipulated by the inserter/impactor 400, such features includethose discussed above as being suitable features on the static trials100 and disc 160, namely, an anteriorly facing flat surface on thesecond (e.g., lower) baseplate of the trial or disc, flanked by twoanteriolaterally facing flat surfaces (one on each side of theanteriorly facing flat surface), and, to provide for holding of thetrial or disc for an anterior insertion approach, a hole spaced from theanteriorly facing flat surface, the hole having a longitudinal axisparallel to the anteriorly facing flat surface.

More particularly, the inserter/impactor 400 includes a shaft 402 havinga distal end 404 that has angled flat surfaces 420 a-c corresponding toand fittable against angled flat surfaces of the static trial (e.g., thesurfaces 120 a-c of the static trial 100) or artificial intervertebraldisc (e.g., the surfaces 180 a-c of the artificial intervertebral disc160) to be implanted. For example, in an anterior approach for the trial100 (as shown in FIGS. 4 e-h), 120 a and 120 d facing 420 a, 120 b and120 e facing 420 b, and 120 c and 120 f facing 420 c, and in an anteriorapproach for the disc 160 (as shown in FIGS. 4 k-n), 180 a and 180 dfacing 420 a, 180 b and 180 e facing 420 b, and 180 c and 180 f facing420 c.

Further, the inserter/impactor 400 includes a holding pin 408 thatextends from the center flat surface 420 b along a longitudinal axis ofthe shaft 402, the pin 408 having a distal end 410 that bends downward.The holding pin 408, is spring loaded (by a spring 409) in a centralchannel of the shaft 402, so that it is biased toward and against thecentral flat surface 420 b (preferably, the bent end 410 of the pin 408prevents it from entering the central channel).

A flange 411, mechanically connected to the pin 408 and translatingadjacent the shaft 402, can be pushed distally to overcome the bias ofthe spring 409 to space the pin 408 away from the central flat surface420 b. In this position, the pin 408 can be inserted in the hole 120b,180 b in the baseplate 108 b,168 b of the static trial 100 orartificial intervertebral disc 160. Releasing the flange 411 allows thespring 409 to pull the pin 408 back, causing the anteriorly facingsurface 120 b,180 b of the baseplate 108 b 168 b to be held against thecentral flat surface 420 b of the inserter/impactor 400 and theanterioloaterally facing flat surfaces 120 a,c,180 a,cof the statictrial 100 or artificial intervertebral disc 160 to be held against theother corresponding flat surfaces 420 a,c of the inserter/impactor 400.A knob 412, threaded on the shaft 402, can be rotated about thelongitudinal axis of the shaft 402 to push the flange 411 fartherproximally, to pull the pin 409 tighter and therefore lock its position(the interference of the threads of the knob-shaft interface preventsthe knob 412 from moving distally unless the knob 412 is reverse rotatedto effect that result) to more securely hold the baseplate 108 b,168 b,and reverse rotated to unlock and loosen the pin 409.

When the static trial 100 or disc 160 is held in this manner, rotationof the static trial 100 or disc 160 about a longitudinal axis (of thestatic trial 100 or disc 160) relative to the inserter/impactor 400 isprevented by interference of the corners of the static trial's 100 ordisc's 160 flat surfaces 120 a-c,180 a-c and the corners of theinserter/impactor's 400 flat surfaces 420 a-c, similar to the manner inwhich a wrench holding a nut prevents rotation of the nut relative tothe wrench. Further, the holding of the static trial 100 or disc 160 inthis manner allows for some repositioning of the static trial 100 ordisc 160 in the intervertebral space via rotation of the static trial100 or disc 160 in either direction about the longitudinal axis of theintervertebral space.

Preferably, both of the baseplates of the static trial 100 or disc 160have similarly configured flat surfaces. For example, the lowerbaseplate's 108 b,168 b flat surfaces 120 a-c,180 a-c have similarlyconfigured and similarly oriented counterpart flat surfaces 120 d-f, 180d-f on the upper baseplate 108 a,168 a. Further preferably, bothbaseplates' 108 a-b, 168 a-b flat surfaces 120 a-f,180 a-f face theangled flat surfaces 420 a-c of the inserter/impactor 400 when thestatic trial 100 or disc 160 is held by the inserter/impactor 400. Forexample, in an anterior approach for the trial 100 (as shown in FIGS. 4e-h), 120 a and 120 d facing 420 a,120 b and 120 e facing 420 b, and 120c and 120 f facing 420 c, and in an anterior approach for the disc 160(as shown in FIGS. 4 k-n), 180 a and 180 d facing 420 a, 180 b and 180 efacing 420 b, and 180 c and 180 f facing 420 c.

It should be noted that preferably, when the static trial 100 is held bythe inserter/impactor 400, the flat surfaces 120 a-c and the counterpartflat surfaces 120 d-f are tightly held against the angled flat surfaces420 a-c of the inserter/impactor 400 as described above. It is alsopreferable that the baseplates 108 a-b of each of the plurality ofstatic trials 100 be appropriately lordotically angled relative to oneanother to ease insertion of the static trial 100 into theintervertebral space and to mimic how the artificial intervertebral disc160 will typically be oriented as it is being inserted using theinserter/impactor 400, and to ease insertion of the static trial 100into the intervertebral space. While not shown in FIGS. 1 a-f, in someembodiments, when the static trials 100 are formed in such alordotically oriented configuration, it is preferable that the flatsurfaces 120 d-f on the first (e.g., upper) baseplate 108 a be parallelto the flat surfaces 120 a-c of the second (e.g., lower) baseplate 108 bin the static trial's 100 appropriately lordotically orientedconfiguration, so that when the static trial 100 is held tightly by theinserter/impactor 400, the flat surfaces 120 a-f are flush with the flatsurfaces 420 a-c of the inserter/impactor 400 even though the baseplates108 a-b are lordotically angled with respect to one another.

By contrast, preferably, when the artificial intervertebral disc 160 isheld by the inserter/impactor 400, the flat surfaces 180 a-c are tightlyheld against the angled flat surfaces 420 a-c of the inserter/impactor400 as described above, but the counterpart flat surfaces 180 d-f areloosely held against the angled flat surfaces 420 a-c of theinserter/impactor 400. As such, the structure of the artificialintervertebral disc 160 having the counterpart flat surfaces 180 d-f(e.g., the upper baseplate 168 a) is able to angulate and rotate to alimited extent relative to the structure of the artificialintervertebral disc 160 having the flat surfaces 180 a-c. This permitsthe artificial intervertebral disc 160 to adjust to the intervertebralspace (e.g., to the angulation of the adjacent vertebral endplates,defining the intervertebral space, relative to one another) as it isbeing inserted thereinto. That is, typically, the adjacent vertebralendplates will be lordotically angled with respect to one another as aresult of the intervertebral space being prepared and distracted. As theartificial intervertebral disc 160 is then inserted into theintervertebral space using the inserter/impactor 400, then, thebaseplates 168 a-b will be permitted to lordotically angle with respectto one another to squeeze into the intervertebral space.

Also preferably, in order to provide for a holding of the static trial100 or disc 160 for two additional (here, anteriolateral) insertionapproaches, each static trial 100 or disc 160 also includes twoadditional holes 122 a,182 a and 122 c,182 c, one (e.g., 122 a,182 a)spaced apart from one of the anteriolaterally facing flat surfaces(e.g., 120 a,180 a), and the other (e.g., 122 c,182 c) spaced apart fromthe other of the anteriolaterally facing flat surfaces (e.g., 120 c,180c). Accordingly, operation of the inserter/impactor 400 can fit theholding pin 408 into either of these two additional holes 122 a,182 a or122 c,182 c, and hold the associated anteriolaterally facing flatsurface (the one associated with the hole into which the pin 408 is fit)of the static trial 100 or disc 160 against the flat surface of theinserter/impactor 400 opposite the pin 408. For example, as discussedbelow with regard to the inserter/impactor 400, in a firstanteriolateral approach for the trial 100 (as shown in FIG. 4 i), 120 aand 120 d facing 420 b, 120 b and 120 e not confronted, and 120 c and120 f facing 420 a, and a first anteriolateral approach for the disc 160(as shown in FIG. 4 o), 180 a and 180 d facing 420 b, 180 b and 180 enot confronted, 180 c and 180 f facing 420 a. And, for example, asdiscussed below with regard to the inserter/impactor 400, in a secondanteriolateral approach for the trial 100 (as shown in FIG. 4 j), 120 aand 120 d facing 420 c, 120 b and 120 e facing 420 a, and 120 c and 120f not confronted, and a second anteriolateral approach for the disc 160(as shown in FIG. 4 p), 180 a and 180 d facing 420 c, 180 b and 180 efacing 420 a, 180 c and 180 f not confronted.

It should be understood that preferably, in order to facilitate theseadditional approaches, the angle separating the anteriorly facing flatsurface of the static trial 100 or disc 160 and one of theanteriolaterally facing flat surfaces of the static trial 100 or disc160 is equal to the angle separating the anteriorly facing flat surfaceand the other of the anteriolaterally facing flat surfaces. Preferably,the surfaces are angled with respect to one another at an angle of 33.4degrees.

It should also be understood that the inclusion of additional adjacentangulated surfaces (or placing the angulated surfaces in other locationson the trial or disc), and/or including corresponding holes adjacent tosuch surfaces, can provide the surgeon with additional approaches, e.g.,other anteriolateral approaches, directly lateral approaches,posteriolateral approaches, and/or directly posterior approaches. Forexample, a trial or disc can have angled surfaces (and correspondingholes), along the entire perimeter of one or both of the baseplates, andthus enable the surgeon to engage the trial or disc from a number ofangles, including anterior, posterior, lateral, anteriolateral, andposteriolateral angles.

The inserter/impactor 400 further includes at a proximal end a cap 414for use as an impact surface if the trial 100 or disc 160 must beimpacted further into the intervertebral space after insertion, orforcibly extracted from the intervertebral space. A mallet can be usedto strike the cap 414 (in a distal direction for impaction, or in aproximal direction (using the flange of the cap 414) for extraction). Itshould be noted a striking of the cap 414 will translate the strikingforce to the baseplates through the shaft 402 and the flat surfaces, butwill not damage the holding pin 408 because the holding pin 408 isspring loaded in the central channel and thus buffered from the strikingforce thereby.

Accordingly, the inserter/impactor 300 can be used to grip either thestatic trials or the artificial intervertebral disc to be implanted, andhold the same during insertion and/or removal of the same, and is usefulfor a variety of surgical approach angles.

Preferred embodiments of a repositioner/extractor of the presentinvention will now be described.

Referring now to FIGS. 5 a-c, a symmetric repositioner/extractor of thepresent invention is shown in side (FIG. 5 a), top (FIG. 5 b), andperspective (FIG. 5 c) views. And referring now to FIGS. 5 d-f, anoffset left repositioner/extractor of the present invention is shown inside (FIG. 5 d), top (FIG. 5 e), and perspective (FIG. 5 f) views. Andreferring now to FIGS. 5 g-i, an offset right repositioner/extractor ofthe present invention is shown in side (FIG. 5 g), top (FIG. 5 h), andperspective (FIG. 5 i) views. And referring now to FIGS. 5 j-l, analternative offset left repositioner/extractor of the present inventionis shown in side (FIG. 5 j), top (FIG. 5 k), and perspective (FIG. 5 l)views. And referring now to FIGS. 5 m-o, an alternative offset rightrepositioner/extractor of the present invention is shown in side (FIG. 5m), top (FIG. 5 n), and perspective (FIG. 5 o) views.

Each repositioner/extractor is provided primarily for repositioningand/or extracting a static trial or artificial intervertebral dischaving features suitable for being manipulated by therepositioner/extractor. Exemplary suitable artificial intervertebraldiscs are described in the '160 application with regard to FIGS. 8 a-y,9 a-t, 10 a-t, 11 a-j, and 12 a-o thereof and by the accompanyingdescriptions therefor (e.g., embodiments identified as the first,second, third, fourth, and fifth preferred embodiments of the fourthembodiment family, etc.). Regarding the features suitable for beingmanipulated by each repositioner/extractor, such features include atleast two holes extending longitudinally into one of the baseplates ofthe static trial or artificial intervertebral disc from the inwardlyfacing surface of the baseplate. More than two holes can be used toprovide for multiple repositioning/extracting approaches. Preferably, inorder for the same repositioning/extracting tool to be used for multipleapproaches on the same trial or artificial intervertebral disc, adjacentholes should be separated by the same distance separating other adjacentholes.

In order to engage the two holes, each repositioner/extractor has twopins extending in parallel from a central shaft, perpendicular to thelongitudinal axis of the central shaft. The pins are spaced to engagethe two holes simultaneously, and each pin has a diameter smaller thanthe diameter of the hole it is to engage. Therefore, the pins can beinserted into the holes, and pulling or pushing on the central shaftalong its longitudinal axis when the holes are engaged pulls or pushesthe static trial or artificial intervertebral disc in the intervertebralspace. Further, because two holes are engaged, the static trial orartificial intervertebral disc can be rotated in either direction abouta longitudinal axis passing through the intervertebral space, byrotating of the central shaft of the repositioner/extractor about itsdistal end, about an axis parallel to the longitudinal axes of the pins.A handle at a proximal end of the central shaft is useful for pushing orpulling on the shaft. A flange adjacent the proximal end of the shaft isuseful for impaction (either with a distally directed force or aproximally directed force), if necessary to manipulate the shaft.

On each repositioner/extractor, the pins are formed on prongs thatextend laterally from the central shaft. The direction of the prongs,and the location of the pins relative to the central shaft, determinethe angle or angles of surgical approach for which a particularrepositioner/extractor can be used. Further, the number and location ofholes further determine the angle or angles of surgical approach forwhich a particular repositioner/extractor can be used. Accordingly, thepresent invention contemplates a variety of repositioner/extractors, anda variety of holes configurations, to provide the surgeon with a varietyof possible surgical approach angles.

For example, three repositioner/extractors are illustrated, and, forexample, two hole configurations are illustrated.

The first, symmetric, repositioner/extractor 500, shown in FIGS. 5 a-c,includes a shaft 502 having a distal end that is symmetrically dividedinto two prongs 504 a-b, each of the prongs having a pin 506 a-bextending upwardly and parallel to the pin on the other prong. Thesecond and third, left offset and right offset, repositioners/extractors510,520, shown in FIGS. 5 d-f and 5 g-i, respectively, each include ashaft 512,522 having a distal end that bends diagonally laterally, theleft offset distal end 514 bending in one direction (e.g., to the left),the right offset distal end 524 bending in an opposite direction (e.g.,to the right). The distal end of each of the second and thirdrepositioners/extractors 510,520 has two pins 516 a-b,526 a-b seriallyspaced on the bent portion, and each of the pins extends upwardly andparallel to the other pin. (As shown in FIGS. 5 j-l and 5 m-o,alternative embodiments 530,540 of the second and third, left offset andright offset, repositioners/extractors each include a shaft 532,542having a distal end that has a straight prong 534 a,544 a and a curvedlateral prong 534 b,544 b, where the curved lateral prong 534 b extendsin one direction (e.g., left) for the alternative left offsetrepositioner/extractor 530, and where the curved lateral prong 544 bextends in an opposite direction (e.g., right) for the alternative rightoffset repositioner/extractor 540. Each of the prongs 534 a-b,544 a-bhas a pin 536 a-b,546 a-b extending upwardly and parallel to the pin onthe other prong. The alternative repositioners/extractors 530,540, eachhaving a space between the pins 536 a,b,546 a,b, provides for avoidanceof any structures on the static trial or artificial intervertebral discthat may be present between the holes.) On each of therepositioners/extractors 500,510,520,530,540, the pins are spaced sothat they simultaneously each fit into a respective one of the twoadjacent holes in the baseplate of the static trial or artificialintervertebral disc. Each of the repositioners/extractors500,510,520,530,540 has a handle 508,518,528,538,548 at a proximal endof the central shaft which is useful for pushing or pulling on theshaft, and a flange 509,519,529,539,549 adjacent the proximal end of theshaft that is useful for impaction (either with a distally directedforce or a proximally directed force), if necessary to manipulate theshaft.

As noted above, the repositioner/extractor that is appropriate ordesired for a given case depends at least in part on the configurationof the holes in the baseplates. Two hole configurations are disclosed,as examples of suitable configurations, although other configurationsare possible and contemplated by the present invention. A first holeconfiguration includes three holes on one of the baseplates, the holesbeing configured so that a first hole is located in theanterior-posterior plane, and the adjacent (second and third) holes arelocated in respective opposing anteriolateral planes on either side ofthe first hole. This hole configuration is shown in FIGS. 5 p-u, each ofwhich shows a top cutaway view of the artificial intervertebral disc ofFIGS. 1 g-n, showing its lower baseplate, having the first holeconfiguration, engaged by one of the repositioners/extractors500,510,520. Each view of the lower baseplate shows the first hole 550,the second hole 552, and the third hole 554 of the first holeconfiguration.

A second hole configuration includes four holes on one of thebaseplates, the holes being configured so that first and second holesstraddle the anterior-posterior plane, a third hole is located so thatthe third hole and the first hole straddle one of the opposinganteriolateral planes, and a fourth hole is located so that the fourthhole and the second hole straddle the other of the opposinganteriolateral planes. This hole configuration is shown in FIGS. 5 v-dd,each of which shows a bottom cutaway view of the artificialintervertebral disc of FIGS. 1 g-n, showing its upper baseplate, havingthe second hole configuration, engaged by one of therepositioners/extractors 500,510,520. Each view of the upper baseplateshows the first hole 560, the second hole 562, the third hole 564, andthe fourth hole 566, of the second hole configuration.

It should be understood that configurations having more or fewer holes,and in a variety of locations, are contemplated by the invention, andthe detailed descriptions of only two hole configurations is not meantto limit the invention to only these two configurations. Importantly,the invention encompasses using a hole or any number of holes, bored atany suitable angle, whether parallel to other holes or not, in anynumber of locations on a spacer, a trial or an artificial intervertebraldisc (not limited to locations on the baseplates), for purposes ofenabling the spacer, trial, or disc to be gripped by a manipulationinstrument (not limited to a repositioner/extractor) that engages thehole, and/or to enable the surgeon to work from a variety of approaches.For example, as described in more detail below, the first and secondhole configurations described herein, in cooperation with therepositioner/extractors, provide the surgeon with the ability to workfrom a directly anterior approach, as well as several anteriolateralapproaches. It should be understood that additional hole configurationscan enable the surgeon to work from a directly posterior approach,posteriolateral approaches, directly lateral approaches, oranteriolateral approaches that are different that those illustrated. Forexample, the placement of one or more suitably spaced holes (or theaddition of one or more holes) on the posterior edge, and/or one or bothof the lateral edges of one or both of the baseplates, would enable thesurgeon to use the repositioner/extractors of the present invention toachieve such approaches.

As noted above, and referring now to FIGS. 5 p-dd, it can be seen thateach of the repositioner/extractors can be used in more than one mannerdepending on the tool desired and the approach desired. For example,with reference to FIGS. 5 p-q, regarding the first hole configuration(three holes in one of the baseplates), the symmetricrepositioner/extractor 500 can be used in either of two anteriolateralapproaches (see FIGS. 5 p-q). That is, the symmetricrepositioner/extractor's shaft 502 can be inserted into the wound fromeither of the two anteriolateral approaches, and the pins 506 a-b can beinserted into the first 550 and second 552 holes (for one of the twoanteriolateral approaches) (FIG. 5 p) or the first 550 and third 552holes (for the other of the two anteriolateral approaches). (FIG. 5 q)of the first hole configuration.

Also, for example, with reference to FIGS. 5 r-u, regarding the firsthole configuration, each of the left offset repositioner/extractor 510and the right offset repositioner/extractor 520 can be used in either adirectly anterior approach (FIGS. 5 r,t) or a respective anteriolateralapproach (FIGS. 5 s,u). That is, the right offsetrepositioner/extractor's shaft 522 can be inserted into the wound from adirect anterior approach, and the right offset repositioner/extractor'spins 526 a-b can then be placed into the first 550 and second 552 holesof the first hole configuration (FIG. 5 r). And, the right offsetrepositioner/extractor's shaft 522 can be inserted into the wound froman anteriolateral approach, and the right offsetrepositioner/extractor's pins 526 a-b can then be placed into the first550 and third 554 holes of the first hole configuration (FIG. 5 s). And,the left offset repositioner/extractor's shaft 512 can be inserted intothe wound from a direct anterior approach, and the left offsetrepositioner/extractor's pins 516 a-b can then be placed into the first550 and third 554 holes of the first hole configuration (FIG. 5 t). And,the left offset repositioner/extractor's shaft 512 can be inserted intothe wound from an anteriolateral approach, and the left offsetrepositioner/extractor's pins 516 a-b can then be placed into the first550 and second 552 holes of the first hole configuration (FIG. 5 u). Itshould be noted that the alternate left offset 530 and alternate rightoffset 540 repositioners/extractors can also fit into the holes of thefirst hole configuration in the same manner as described here withregard to the left offset 510 and right offset 520repositioners/extractors.

Also, for example, with reference to FIGS. 5

v-dd, regarding the second hole configuration (four holes in one of thebaseplates), the symmetric repositioner/extractor 500 can be used in adirectly anterior approach (FIG. 5 v), and either of two anteriolateralapproaches (FIGS. 5 w-x). That is, the symmetricrepositioner/extractor's shaft 502 can be inserted into the wound from adirectly anterior approach, and the pins 506 a-b can be inserted intothe first 560 and second 562 holes of the second hole configuration(FIG. 5 v). And, the symmetric repositioner/extractor's shaft 502 can beinserted into the wound from either of the two anteriolateralapproaches, and the pins 506 a-b can be inserted into the first 560 andthird 564 holes (for one of the two anteriolateral approaches) (FIG. 5w) or the second 562 and fourth 566 holes (for the other of the twoanteriolateral approaches) (FIG. 5 x) of the second hole configuration.

Also, for example, with reference to FIGS. 5 y-dd, regarding the secondhole configuration, each of the left offset repositioner/extractor 510and the right offset repositioner/extractor 520 can be used in any ofthree respective anteriolateral approaches. That is, the right offsetrepositioner/extractor's shaft 522 can be inserted into the wound fromany of its three possible anteriolateral approaches, and the rightoffset repositioner/extractor's pins 526 a-b can then be placed into thefirst 560 and second 562 holes (FIG. 5 y) (for a first of the threeanteriolateral approaches), the first 560 and third 564 holes (FIG. 5 z)(for a second of the three anteriolateral approaches), or the second 562and fourth 566 holes (FIG. 5 aa) (for a third of the threeanteriolateral approaches). And, the left offsetrepositioner/extractor's shaft 512 can be inserted into the wound fromany of its three possible anteriolateral approaches, and the left offsetrepositioner/extractor's pins 516 a-b can then be placed into the first560 and second 562 holes (FIG. 5 bb) (for a first of the threeanteriolateral approaches), the first 560 and third 564 holes (FIG. 5cc) (for a second of the three anteriolateral approaches), or the second562 and fourth 566 holes (FIG. 5 dd) (for a third of the threeanteriolateral approaches). It should be noted that the alternate leftoffset 530 and alternate right offset 540 repositioners/extractors canalso fit into the holes of the second hole configuration in the samemanner as described here with regard to the left offset 510 and rightoffset 520 repositioners/extractors.

It should be noted from the illustrations in FIGS. 5 p-dd that theanteriolateral approaches are at a variety of angles relative to theanterior-posterior plane, and further that the illustrated angles aremerely exemplary. That is, the invention encompasses additional approachangles, in that such additional approach angles are possible by (asdescribed above) adding or deleting holes, and/or changing the locationof holes, and/or changing the spacing between holes (in conjunction withchanging the spacing between pins), and/or changing the angle at whichthe offset repositioner/extractors' pins are placed relative to oneanother and to the shaft of such repositioner/extractors.

As discussed above, once the pins are established in the two adjacentholes, manipulating the shaft of the repositioner/extractor willreposition the static trial or artificial intervertebral disc in theintervertebral space and/or extract it from the intervertebral space.The use of more than one pin (versus one pin) enables the static trialor artificial intervertebral disc to be rotated in either directionabout a longitudinal axis passing through the intervertebral space.

A preferred embodiment of a leveler of the present invention will now bedescribed.

Referring now to FIGS. 6 a-e, a leveler of the present invention isshown in bottom (FIG. 6 a), side (FIG. 6 b), front (FIG. 6 c), toppartial perspective (FIG. 6 d), and bottom partial perspective (FIG. 6e) views. More particularly, FIG. 6 d shows a top perspective view ofthe distal end of the leveler, and FIG. 6 e shows a bottom perspectiveview of the distal end of the leveler.

The leveler is provided primarily for establishing a parallelorientation of the baseplates (relative to one another), and/or securingthe purchase of the stabilizing spikes, of an artificial intervertebraldisc having features suitable for being manipulated by the leveler.Exemplary suitable artificial intervertebral discs are described in the'160 application with regard to FIGS. 8 a-y, 9 a-t, 10 a-t, 11 a-j, and12 a-o thereof and by the accompanying descriptions therefor (e.g.,embodiments identified as the first, second, third, fourth, and fifthpreferred embodiments of the fourth embodiment family, etc.). Regardingthe features suitable for being manipulated by the leveler, suchfeatures include suitably formed inwardly facing surfaces of thebaseplates of the artificial intervertebral disc.

More particularly, the leveler 600 includes a shaft 602 having a forkeddistal end formed by two opposing tongs 604 a-b that are symmetric toone another about a longitudinal axis of the shaft 602. Each of thetongs 604 a-b has an extent that initially curves laterally outward awayfrom the shaft 602 and from the other tong's extent, to define a centralpocket 606 forward of the shaft 602 between the tongs' extents. Eachtong's extent then resumes a distal direction to become parallel to theshaft 602 and to the other tong's extent.

Each tong's extent has an upper surface 608 a-b and a lower surface 610a-b. The upper surface 608 a-b is preferably shaped to conform againstthe inwardly facing surface of a first (e.g., upper) baseplate of anartificial intervertebral disc, and the lower surface 610 a-b ispreferably shaped to conform against the inwardly facing surface of asecond (e.g., lower) baseplate of the artificial intervertebral disc, sothat insertion of the forked distal end of the leveler 600 between thebaseplates, with the central pocket 606 of the distal end avoiding thecentral portion of the artificial intervertebral disc, and with theupper 608 a-b and lower surfaces 610 a-b so engaging the inwardly facingsurfaces of the baseplates, causes the baseplates to be placed inparallel orientation with respect to one another.

More particularly, for example for use with the exemplary artificialintervertebral disc of FIGS. 1 g-n, the upper surface 608 a-b of eachextent is flat, except for a tapered section 612 a-b at the distal tipof the extent, which tapered section narrows the tip, and the lowersurface 610 a-b of each extent is curved to form opposing concavecontours 614 a-b that are cooperatingly shaped to conform against theinwardly facing surface of the convex structure of the artificialintervertebral disc.

The preferred use of the leveler 600 is as follows. As discussed above,once the intervertebral space has been prepared and distracted to adimension that will accept the artificial intervertebral disc to beimplanted, the artificial intervertebral disc 160 is engaged at itslower baseplate 168 b by the inserter/impactor 400 discussed above.During insertion (and, if necessary, impaction) of the artificialintervertebral disc 160 into the intervertebral space, the upperbaseplate 168 a remains free to angulate with respect to the lowerbaseplate 168 b, so that the angulation of the baseplates conforms tothe angulation of the intervertebral space as the artificialintervertebral disc is being inserted thereinto. Typically, theendplates of the prepared and distracted intervertebral space will belordotically angled with respect to one another, due to the use of thestatic trials 100 as described above, which are formed to have alordotic taper as discussed above. Thus, when the artificialintervertebral disc is inserted into the intervertebral space, itsbaseplates will be lordotically angled with respect to one another. Oncethe artificial intervertebral disc 160 is inserted, theinserter/impactor 400 can be disengaged, and the repositioner/extractors500,510,520,530,540 discussed above can be applied to the artificialintervertebral disc, if necessary to achieve a more optimal positioning.

Once the positioning is established, the leveler 600 is preferablyapplied to the artificial intervertebral disc 160. The forked distal endof the leveler 600 is inserted so that the extents 604 a-b are placedbetween the inwardly facing surface 164 a of the upper baseplate 168 aand the inwardly facing surface 164 b of the convex structure 162 on thelower baseplate 168 b, and so that the central pocket 606 of the leveler600 avoids the ball-and-socket joint of the artificial intervertebraldisc 160. If the baseplates are lordotically angled with respect to oneanother, the tapered sections 612 a-b of the upper surfaces 608 a-b ofthe forked distal end will be approximately parallel to, and will firstencounter, the angled inwardly facing surface 164 a of the upperbaseplate 168 a. At the same time, the concave contours 614 a-b of thelower surfaces 610 a-b will accommodate the inwardly facing surface 164b of the convex structure 162 on the lower baseplate 168 b. As thetapered sections 612 a-b press against the inwardly facing surface 164 aof the upper baseplate 168 a, and the concave contours 614 a-b slip intoplace against the inwardly facing surface 164 b of the convex structure162 on the lower baseplate 168 b, the tapers 612 a-b will function aswedges to force the posterior portion of the upper baseplate 168 a awayfrom the posterior portion of the lower baseplate 168 b. Accordingly, asthe posterior portions are being separated, the stabilizing spikes 188a-b on the outwardly facing surfaces 186 a-b of the baseplates 168 a-bfind or secure their purchase in the hard bone of the outer ring of thevertebral body endplates. When the forked distal end is fully seated(stops 616 a-b are provided to butt up against the anterior portions ofthe baseplates 168 a-b to prevent the forked distal end from beinginserted too far), the extents of the tongs 604 a-b hold the baseplates168 a-b parallel to one another, and so that the spikes 188 a-b arefully engaged in the endplates. The surgeon then slips the leveler 600out from between the baseplates 168 a-b, and out from the wound andcompletes the procedure. A handle 618 is provided at a proximal end ofthe shaft 602 for pushing, pulling, and otherwise manipulating theleveler 600 as needed.

While there has been described and illustrated specific embodiments ofinstrumentation, it will be apparent to those skilled in the art thatvariations and modifications are possible without deviating from thebroad spirit and principle of the invention. The invention, therefore,shall not be limited to the specific embodiments discussed herein.

1. An apparatus for manipulating a preparation device for preparing anintervertebral space, the apparatus comprising: an extension having alongitudinal axis; at least two prongs coupled to a fulcrum located at adistal extension end of the extension, each of the prongs having a prongextension, the prong extensions together defining a contractable andexpandable holding enclosure for holding the preparation device; and asleeve that surrounds at least a portion of the distal extension endincluding the fulcrum and at least a portion of the two prongs, thesleeve being collinear with the extension longitudinal axis, fixed inboth proximal and distal directions with respect to the longitudinalaxis, and rotatable about the extension longitudinal axis; said sleevehaving a bore that extends along the longitudinal axis of the extension,the bore defining a crosssection on a plane perpendicular to thelongitudinal axis of the extension, the crosssection having a width thatis greater than a depth, wherein when the sleeve is rotated about theextension longitudinal axis the sleeve remains longitudinally fixed andthe sides of the bore defining the depth of the crosssection bear on atleast one of the prongs to move the holding enclosure to a contractedstate in which the preparation device cannot be removed from the holdingenclosure.
 2. The apparatus according to claim 1, wherein themanipulating includes at least one of holding, inserting, repositioning,removing, impacting, and extracting.
 3. The apparatus according to claim1, further comprising a handle having a distal handle end coupled to aproximal extension end of the extension.
 4. The apparatus according toclaim 1, further comprising a flange that facilitates the rotation ofthe sleeve.
 5. The apparatus according to claim 1, wherein the holdingenclosure is cylindrical.
 6. The apparatus of claim 1, wherein a firstof the prongs is springloaded with respect to a second of the prongs tobias the holding enclosure to a receptive state in which the first prongand the second prong are separated by a receptive state distance thatdoes not allow an desired engagement diameter of the preparation deviceto pass between a first prong distal end of the first prong and a secondprong distal end of the second prong without altering a position of atleast one of the prongs; wherein a manual pushing, using a force greatenough to overcome the bias, of the preparation device in a proximaldirection along the extension longitudinal axis between the first prongdistal end and the second prong distal end brings the holding enclosureto an expanded state in which the first prong and the second prong areseparated by an expanded state distance that allows the desiredengagement diameter of the preparation device to completely pass betweenthe first prong distal end and the second prong distal end, the spacingand dimensioning of the two prongs relative to the sleeve permittingsuch bringing of the holding enclosure to the expanded state; andwherein rotation of the sleeve about the extension longitudinal axisbrings an inner surface of the sleeve to bear on at least one of theprongs to move the holding enclosure to a contracted state in which theholding enclosure cannot be brought to the expanded state.
 7. Theapparatus according to claim 6, wherein the springloading of the prongsrelative to one another is effected by at least one of a dimension of atleast one of the prongs or a material strength of at least one of theprongs.
 8. The apparatus according to claim 6, wherein the distalextension ends are tapered more narrowly toward the holding enclosure tofacilitate passage of the preparation device therethrough.
 9. Theapparatus of claim 1, wherein the sleeve is biased toward stopping itsrotation at desired positions.
 10. The apparatus of claim 9, wherein thebiasing is effected by at least one plunger and at least one recesscooperating with the plunger at the desired position.
 11. The apparatusaccording to claim 10, wherein at least one recess is located on anouter surface of the extension, at least one sleeve wall bore penetratesthrough a wall of the sleeve; and at least one plunger is located withinat least a portion of at least one of the sleeve wall bores; wherein atleast one of the plungers is biased from an inner sleeve surface of thesleeve radially inward toward a longitudinal sleeve axis of the sleeve;wherein as the sleeve rotates about the longitudinal extension axis ofthe extension, at least one of the plungers aligns with at least one ofthe recesses allowing at least one of the plungers to expand radiallyinward such that at least a portion of at least one of the plungers iscontained with at least a portion of at least one of the recesses. 12.An apparatus according to claim 11, wherein the plunger includes aspring.
 13. An apparatus according to claim 1, wherein aligningoutwardly facing surfaces of the at least two prongs longitudinallyalong the sleeve bore width allows the prongs to expand fully withoutinterfering with an inner surface of the sleeve bore; and whereinaligning the outwardly facing surfaces of the at least two prongslongitudinally along the sleeve bore depth causes interference betweenat least one of the outwardly facing surfaces of at least one of theprongs and at least one of the inner surfaces of the sleeve bore.
 14. Anapparatus according to claim 13, wherein at least one of the sleevebores includes at least one corner having a corner curvature shaped as aradius of the sleeve bore; and wherein at least one outwardly facingsurface of at least one of the prongs is curved such that the curvedprong and the corner curvature facilitate the rotation of the sleeve.15. An apparatus according to claim 1, wherein the at least one prongextension widens outwardly.
 16. An apparatus according to claim 1,wherein the at least one prong extension is ridged.
 17. An apparatusaccording to claim 1, wherein the at least one prong extension includesa first semicircular extension having a first inwardly facing surfaceand a second semicircular extension having a second inwardly facingsurface that faces the first inwardly facing surface such that the firstand second inwardly facing surfaces form the holding enclosure.
 18. Anapparatus according to claim 17, wherein the rotation of the sleevecontracts and expands the first and second inwardly facing surfacesrelative to each other.